Canonical Allele Identifier: CA2712658370
Gene: SOBP HGNC NCBI

Linked Data

dbSNP Id: rs2115146507

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634537_107634548del , CM000668.2:g.107634537_107634548del GRCh38
NC_000006.11:g.107955741_107955752del , CM000668.1:g.107955741_107955752del GRCh37
NC_000006.10:g.108062434_108062445del NCBI36
NG_028200.1:g.149425_149436del
NG_028200.2:g.149425_149436del

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1693_1704del MANE Select ENSP00000318900.5:p.Asn565_Gly568del
ENST00000317357.9:c.1693_1704del ENSP00000318900.5:p.Asn565_Gly568del
NM_018013.3:c.1693_1704del NP_060483.3:p.Asn565_Gly568del
XM_005267041.3:c.1846_1857del XP_005267098.1:p.Asn616_Gly619del
XM_005267042.3:c.1750_1761del XP_005267099.1:p.Asn584_Gly587del
XM_011535920.1:c.1846_1857del XP_011534222.1:p.Asn616_Gly619del
XM_011535921.1:c.1732_1743del XP_011534223.1:p.Asn578_Gly581del
XM_011535922.1:c.1105_1116del XP_011534224.1:p.Asn369_Gly372del
XM_011535923.1:c.916_927del XP_011534225.1:p.Asn306_Gly309del
XM_005267041.4:c.1846_1857del XP_005267098.1:p.Asn616_Gly619del
XM_005267042.4:c.1750_1761del XP_005267099.1:p.Asn584_Gly587del
XM_011535920.2:c.1846_1857del XP_011534222.1:p.Asn616_Gly619del
XM_011535921.2:c.1732_1743del XP_011534223.1:p.Asn578_Gly581del
XM_011535923.2:c.916_927del XP_011534225.1:p.Asn306_Gly309del
XM_017010991.1:c.1246_1257del XP_016866480.1:p.Asn416_Gly419del
XM_017010992.1:c.1246_1257del XP_016866481.1:p.Asn416_Gly419del
XM_017010993.1:c.1246_1257del XP_016866482.1:p.Asn416_Gly419del
XM_017010994.1:c.1246_1257del XP_016866483.1:p.Asn416_Gly419del
NM_018013.4:c.1693_1704del MANE Select NP_060483.3:p.Asn565_Gly568del