Canonical Allele Identifier: CA397045705

Gene: BANP

Linked Data

• ClinVar Variation Id: 487782
• ClinVar RCV Id: RCV000577856
• dbSNP Id: rs1555586650
• MyVariant Identifiers: chr16:g.88052070A>G (hg19) ; chr16:g.88018464A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88018464A>G , CM000678.2:g.88018464A>G	GRCh38
NC_000016.9:g.88052070A>G , CM000678.1:g.88052070A>G	GRCh37
NC_000016.8:g.86609571A>G	NCBI36
NG_029918.1:g.72033A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700483.1:c.692A>G	ENSP00000515015.1:p.Asn231Ser
ENST00000682872.1:c.692A>G MANE Select	ENSP00000507916.1:p.Asn231Ser
ENST00000286122.11:c.668A>G	ENSP00000286122.7:p.Asn223Ser
ENST00000355022.8:c.575A>G	ENSP00000347125.4:p.Asn192Ser
ENST00000393207.5:c.668A>G	ENSP00000376902.1:p.Asn223Ser
ENST00000393208.6:c.575A>G	ENSP00000376903.2:p.Asn192Ser
ENST00000479780.6:c.575A>G	ENSP00000432508.1:p.Asn192Ser
ENST00000497491.1:n.257A>G
ENST00000538234.5:c.692A>G	ENSP00000444352.1:p.Asn231Ser
ENST00000626016.2:c.593A>G	ENSP00000487304.1:p.Asn198Ser
NM_001173539.1:c.692A>G	NP_001167010.1:p.Asn231Ser
NM_001173540.1:c.593A>G	NP_001167011.1:p.Asn198Ser
NM_001173541.1:c.575A>G	NP_001167012.1:p.Asn192Ser
NM_001173542.1:c.692A>G	NP_001167013.1:p.Asn231Ser
NM_001173543.1:c.668A>G	NP_001167014.1:p.Asn223Ser
NM_017869.3:c.575A>G	NP_060339.2:p.Asn192Ser
NM_079837.2:c.575A>G	NP_524576.2:p.Asn192Ser
XM_005256008.2:c.710A>G	XP_005256065.1:p.Asn237Ser
XM_005256009.2:c.692A>G	XP_005256066.1:p.Asn231Ser
XM_011523170.1:c.710A>G	XP_011521472.1:p.Asn237Ser
XM_011523171.1:c.710A>G	XP_011521473.1:p.Asn237Ser
XM_011523172.1:c.710A>G	XP_011521474.1:p.Asn237Ser
XM_011523173.1:c.710A>G	XP_011521475.1:p.Asn237Ser
XM_011523174.1:c.710A>G	XP_011521476.1:p.Asn237Ser
XM_011523175.1:c.710A>G	XP_011521477.1:p.Asn237Ser
XM_011523176.1:c.710A>G	XP_011521478.1:p.Asn237Ser
XM_011523177.1:c.710A>G	XP_011521479.1:p.Asn237Ser
XM_011523178.1:c.710A>G	XP_011521480.1:p.Asn237Ser
XM_011523179.1:c.692A>G	XP_011521481.1:p.Asn231Ser
XM_011523180.1:c.692A>G	XP_011521482.1:p.Asn231Ser
XM_011523181.1:c.710A>G	XP_011521483.1:p.Asn237Ser
XM_011523182.1:c.710A>G	XP_011521484.1:p.Asn237Ser
XM_011523183.1:c.383A>G	XP_011521485.1:p.Asn128Ser
XM_011523184.1:c.347A>G	XP_011521486.1:p.Asn116Ser
XM_011523185.1:c.266A>G	XP_011521487.1:p.Asn89Ser
XM_011523186.1:c.-11A>G	XP_011521488.1:n.-11A>G
XM_011523187.1:c.692A>G	XP_011521489.1:p.Asn231Ser
XR_933350.1:n.860A>G
XR_933352.1:n.860A>G
XR_933353.1:n.860A>G
XR_933355.1:n.860A>G
XR_933356.1:n.860A>G
XR_933357.1:n.860A>G
XR_933358.1:n.860A>G
XR_933359.1:n.860A>G
XR_933360.1:n.860A>G
XM_005256008.3:c.710A>G	XP_005256065.1:p.Asn237Ser
XM_005256009.4:c.692A>G	XP_005256066.1:p.Asn231Ser
XM_011523170.2:c.710A>G	XP_011521472.1:p.Asn237Ser
XM_011523172.2:c.710A>G	XP_011521474.1:p.Asn237Ser
XM_011523174.2:c.710A>G	XP_011521476.1:p.Asn237Ser
XM_011523175.3:c.710A>G	XP_011521477.1:p.Asn237Ser
XM_011523176.2:c.710A>G	XP_011521478.1:p.Asn237Ser
XM_011523177.2:c.710A>G	XP_011521479.1:p.Asn237Ser
XM_011523178.2:c.710A>G	XP_011521480.1:p.Asn237Ser
XM_011523179.3:c.692A>G	XP_011521481.1:p.Asn231Ser
XM_011523180.2:c.692A>G	XP_011521482.1:p.Asn231Ser
XM_011523181.2:c.710A>G	XP_011521483.1:p.Asn237Ser
XM_011523183.2:c.383A>G	XP_011521485.1:p.Asn128Ser
XM_011523184.2:c.347A>G	XP_011521486.1:p.Asn116Ser
XM_017023378.1:c.710A>G	XP_016878867.1:p.Asn237Ser
XM_017023379.2:c.692A>G	XP_016878868.1:p.Asn231Ser
XM_017023380.2:c.575A>G	XP_016878869.1:p.Asn192Ser
XM_017023381.1:c.593A>G	XP_016878870.1:p.Asn198Ser
XM_017023382.1:c.116A>G	XP_016878871.1:p.Asn39Ser
XM_017023383.2:c.-11A>G	XP_016878872.1:n.-11A>G
XM_024450320.1:c.692A>G	XP_024306088.1:p.Asn231Ser
XM_024450321.1:c.692A>G	XP_024306089.1:p.Asn231Ser
XM_024450322.1:c.692A>G	XP_024306090.1:p.Asn231Ser
XM_024450323.1:c.692A>G	XP_024306091.1:p.Asn231Ser
XM_024450324.1:c.692A>G	XP_024306092.1:p.Asn231Ser
XM_024450325.1:c.710A>G	XP_024306093.1:p.Asn237Ser
XM_024450326.1:c.575A>G	XP_024306094.1:p.Asn192Ser
XM_024450327.1:c.383A>G	XP_024306095.1:p.Asn128Ser
XM_024450328.1:c.347A>G	XP_024306096.1:p.Asn116Ser
XM_024450329.1:c.266A>G	XP_024306097.1:p.Asn89Ser
XM_024450330.1:c.266A>G	XP_024306098.1:p.Asn89Ser
XM_024450331.1:c.-11A>G	XP_024306099.1:n.-11A>G
XM_024450332.1:c.-11A>G	XP_024306100.1:n.-11A>G
XM_024450333.1:c.-11A>G	XP_024306101.1:n.-11A>G
XM_024450334.1:c.-11A>G	XP_024306102.1:n.-11A>G
XR_001751945.1:n.860A>G
XR_001751946.1:n.860A>G
XR_001751947.1:n.860A>G
XR_001751948.1:n.860A>G
XR_933350.2:n.860A>G
XR_933352.2:n.860A>G
XR_933353.2:n.860A>G
NM_001173539.2:c.692A>G	NP_001167010.1:p.Asn231Ser
NM_001173540.2:c.593A>G	NP_001167011.1:p.Asn198Ser
NM_001173541.2:c.575A>G	NP_001167012.1:p.Asn192Ser
NM_017869.4:c.575A>G	NP_060339.2:p.Asn192Ser
NM_079837.3:c.575A>G	NP_524576.2:p.Asn192Ser
NM_001384916.1:c.575A>G	NP_001371845.1:p.Asn192Ser
NM_001384918.1:c.692A>G	NP_001371847.1:p.Asn231Ser
NM_001384919.1:c.692A>G	NP_001371848.1:p.Asn231Ser
NM_001384920.1:c.692A>G	NP_001371849.1:p.Asn231Ser
NM_001384921.1:c.575A>G	NP_001371850.1:p.Asn192Ser
NM_001384922.1:c.575A>G	NP_001371851.1:p.Asn192Ser
NM_001384923.1:c.575A>G	NP_001371852.1:p.Asn192Ser
NM_001384925.1:c.692A>G	NP_001371854.1:p.Asn231Ser
NM_001384926.1:c.692A>G	NP_001371855.1:p.Asn231Ser
NM_001384927.1:c.692A>G	NP_001371856.1:p.Asn231Ser
NM_001384928.1:c.710A>G	NP_001371857.1:p.Asn237Ser
NM_001384929.1:c.710A>G	NP_001371858.1:p.Asn237Ser
NM_001384931.1:c.710A>G	NP_001371860.1:p.Asn237Ser
NM_001384935.1:c.710A>G	NP_001371864.1:p.Asn237Ser
NM_001384936.1:c.593A>G	NP_001371865.1:p.Asn198Ser
NM_001384937.1:c.593A>G	NP_001371866.1:p.Asn198Ser
NM_001384938.1:c.593A>G	NP_001371867.1:p.Asn198Ser
NM_001384939.1:c.383A>G	NP_001371868.1:p.Asn128Ser
NM_001384940.1:c.383A>G	NP_001371869.1:p.Asn128Ser
NM_001384941.1:c.383A>G	NP_001371870.1:p.Asn128Ser
NM_001384942.1:c.383A>G	NP_001371871.1:p.Asn128Ser
NM_001384943.1:c.266A>G	NP_001371872.1:p.Asn89Ser
NM_001384944.1:c.266A>G	NP_001371873.1:p.Asn89Ser
NM_001386991.1:c.692A>G MANE Select	NP_001373920.1:p.Asn231Ser
NM_001386992.1:c.692A>G	NP_001373921.1:p.Asn231Ser