Canonical Allele Identifier: CA1435774034
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301566_6301567delinsTC , CM000666.2:g.6301566_6301567delinsTC GRCh38
NC_000004.11:g.6303293_6303294delinsTC , CM000666.1:g.6303293_6303294delinsTC GRCh37
NC_000004.10:g.6354194_6354195delinsTC NCBI36
NG_011700.1:g.36717_36718delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1807_1808delinsTC ENSP00000507852.1:p.Ser603=
ENST00000683395.1:c.1748_1749delinsTC
ENST00000684087.1:c.1771_1772delinsTC ENSP00000506978.1:p.Ser591=
ENST00000506362.2:c.1522_1523delinsTC ENSP00000424103.2:p.Ser508=
ENST00000673642.1:c.1430_1431delinsTC ENSP00000501242.1:n.1430_1431delinsTC
ENST00000673991.1:c.1807_1808delinsTC ENSP00000501033.1:p.Ser603=
ENST00000226760.5:c.1771_1772delinsTC MANE Select ENSP00000226760.1:p.Ser591=
ENST00000503569.5:c.1771_1772delinsTC ENSP00000423337.1:p.Ser591=
ENST00000507765.1:n.1956_1957delinsTC
NM_001145853.1:c.1771_1772delinsTC NP_001139325.1:p.Ser591=
NM_006005.3:c.1771_1772delinsTC MANE Select NP_005996.2:p.Ser591=
XM_017008586.1:c.1780_1781delinsTC XP_016864075.1:p.Ser594=