Canonical Allele Identifier: CA91796396

Gene: WFS1

Linked Data

• dbSNP Id: rs867112112
• gnomAD v2: 4-6303136-C-T
• gnomAD v4: 4-6301409-C-T
• MyVariant Identifiers: chr4:g.6303136C>T (hg19) ; chr4:g.6301409C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301409C>T , CM000666.2:g.6301409C>T	GRCh38
NC_000004.11:g.6303136C>T , CM000666.1:g.6303136C>T	GRCh37
NC_000004.10:g.6354037C>T	NCBI36
NG_011700.1:g.36560C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1650C>T	ENSP00000507852.1:p.Phe550=
ENST00000683395.1:c.1591C>T
ENST00000684087.1:c.1614C>T	ENSP00000506978.1:p.Phe538=
ENST00000506362.2:c.1365C>T	ENSP00000424103.2:p.Phe455=
ENST00000673642.1:c.1273C>T	ENSP00000501242.1:p.His425Tyr
ENST00000673991.1:c.1650C>T	ENSP00000501033.1:p.Phe550=
ENST00000226760.5:c.1614C>T MANE Select	ENSP00000226760.1:p.Phe538=
ENST00000503569.5:c.1614C>T	ENSP00000423337.1:p.Phe538=
ENST00000507765.1:n.1799C>T
NM_001145853.1:c.1614C>T	NP_001139325.1:p.Phe538=
NM_006005.3:c.1614C>T MANE Select	NP_005996.2:p.Phe538=
XM_017008586.1:c.1623C>T	XP_016864075.1:p.Phe541=