Canonical Allele Identifier: CA352517357

Gene: NBEAL2

Linked Data

• MyVariant Identifiers: chr3:g.47041878A>G (hg19) ; chr3:g.47000388A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000388A>G , CM000665.2:g.47000388A>G	GRCh38
NC_000003.11:g.47041878A>G , CM000665.1:g.47041878A>G	GRCh37
NC_000003.10:g.47016882A>G	NCBI36
NG_031914.1:g.25706A>G , LRG_568:g.25706A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.4289A>G MANE Select	ENSP00000415034.2:p.Asn1430Ser
ENST00000651747.1:c.4187A>G	ENSP00000499216.1:p.Asn1396Ser
ENST00000416683.5:c.2152A>G
ENST00000450053.7:c.4289A>G	ENSP00000415034.2:p.Asn1430Ser
NM_015175.2:c.4289A>G , LRG_568t1:c.4289A>G	NP_055990.1:p.Asn1430Ser
XM_005264992.2:c.4187A>G	XP_005265049.1:p.Asn1396Ser
XM_005264993.2:c.761A>G	XP_005265050.1:p.Asn254Ser
XM_006713072.2:c.4208A>G	XP_006713135.1:p.Asn1403Ser
XM_011533532.1:c.4268A>G	XP_011531834.1:p.Asn1423Ser
XM_011533533.1:c.4289A>G	XP_011531835.1:p.Asn1430Ser
XM_011533534.1:c.3920A>G	XP_011531836.1:p.Asn1307Ser
XM_011533535.1:c.3749A>G	XP_011531837.1:p.Asn1250Ser
XM_011533536.1:c.3635A>G	XP_011531838.1:p.Asn1212Ser
XM_011533537.1:c.3197A>G	XP_011531839.1:p.Asn1066Ser
XR_940397.1:n.4465A>G
XR_940398.1:n.4465A>G
NM_001365116.1:c.4187A>G	NP_001352045.1:p.Asn1396Ser
XM_006713072.3:c.4208A>G	XP_006713135.1:p.Asn1403Ser
XM_011533533.2:c.4289A>G	XP_011531835.1:p.Asn1430Ser
XM_017006010.1:c.4289A>G	XP_016861499.1:p.Asn1430Ser
XM_017006011.1:c.4268A>G	XP_016861500.1:p.Asn1423Ser
XM_017006012.1:c.4208A>G	XP_016861501.1:p.Asn1403Ser
XM_017006013.1:c.4289A>G	XP_016861502.1:p.Asn1430Ser
XM_017006014.1:c.4187A>G	XP_016861503.1:p.Asn1396Ser
XM_017006015.1:c.3920A>G	XP_016861504.1:p.Asn1307Ser
XM_017006016.1:c.3749A>G	XP_016861505.1:p.Asn1250Ser
XM_017006017.1:c.761A>G	XP_016861506.1:p.Asn254Ser
XR_940397.2:n.4465A>G
NM_001365116.2:c.4187A>G	NP_001352045.1:p.Asn1396Ser
NM_015175.3:c.4289A>G MANE Select	NP_055990.1:p.Asn1430Ser