Canonical Allele Identifier: CA1435773116
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301287_6301290delinsGTCC , CM000666.2:g.6301287_6301290delinsGTCC GRCh38
NC_000004.11:g.6303014_6303017delinsGTCC , CM000666.1:g.6303014_6303017delinsGTCC GRCh37
NC_000004.10:g.6353915_6353918delinsGTCC NCBI36
NG_011700.1:g.36438_36441delinsGTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1528_1531delinsGTCC ENSP00000507852.1:p.Val510=
ENST00000683395.1:c.1469_1472delinsGTCC
ENST00000684087.1:c.1492_1495delinsGTCC ENSP00000506978.1:p.Val498=
ENST00000506362.2:c.1243_1246delinsGTCC ENSP00000424103.2:p.Val415=
ENST00000673642.1:c.1151_1154delinsGTCC ENSP00000501242.1:p.Arg384=
ENST00000673991.1:c.1528_1531delinsGTCC ENSP00000501033.1:p.Val510=
ENST00000226760.5:c.1492_1495delinsGTCC MANE Select ENSP00000226760.1:p.Val498=
ENST00000503569.5:c.1492_1495delinsGTCC ENSP00000423337.1:p.Val498=
ENST00000507765.1:n.1677_1680delinsGTCC
NM_001145853.1:c.1492_1495delinsGTCC NP_001139325.1:p.Val498=
NM_006005.3:c.1492_1495delinsGTCC MANE Select NP_005996.2:p.Val498=
XM_017008586.1:c.1501_1504delinsGTCC XP_016864075.1:p.Val501=