Canonical Allele Identifier: CA356175170
Gene: WFS1 HGNC NCBI

Linked Data

gnomAD v4: 4-6301287-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301287G>T , CM000666.2:g.6301287G>T GRCh38
NC_000004.11:g.6303014G>T , CM000666.1:g.6303014G>T GRCh37
NC_000004.10:g.6353915G>T NCBI36
NG_011700.1:g.36438G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1528G>T ENSP00000507852.1:p.Val510Phe
ENST00000683395.1:c.1469G>T
ENST00000684087.1:c.1492G>T ENSP00000506978.1:p.Val498Phe
ENST00000506362.2:c.1243G>T ENSP00000424103.2:p.Val415Phe
ENST00000673642.1:c.1151G>T ENSP00000501242.1:p.Arg384Leu
ENST00000673991.1:c.1528G>T ENSP00000501033.1:p.Val510Phe
ENST00000226760.5:c.1492G>T MANE Select ENSP00000226760.1:p.Val498Phe
ENST00000503569.5:c.1492G>T ENSP00000423337.1:p.Val498Phe
ENST00000507765.1:n.1677G>T
NM_001145853.1:c.1492G>T NP_001139325.1:p.Val498Phe
NM_006005.3:c.1492G>T MANE Select NP_005996.2:p.Val498Phe
XM_017008586.1:c.1501G>T XP_016864075.1:p.Val501Phe