Canonical Allele Identifier: CA356174141

Gene: WFS1

Linked Data

• dbSNP Id: rs1297069854
• gnomAD v2: 4-6302568-T-C
• gnomAD v4: 4-6300841-T-C
• MyVariant Identifiers: chr4:g.6302568T>C (hg19) ; chr4:g.6300841T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300841T>C , CM000666.2:g.6300841T>C	GRCh38
NC_000004.11:g.6302568T>C , CM000666.1:g.6302568T>C	GRCh37
NC_000004.10:g.6353469T>C	NCBI36
NG_011700.1:g.35992T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1082T>C	ENSP00000507852.1:p.Ile361Thr
ENST00000683395.1:c.1023T>C
ENST00000684087.1:c.1046T>C	ENSP00000506978.1:p.Ile349Thr
ENST00000506362.2:c.797T>C	ENSP00000424103.2:p.Ile266Thr
ENST00000673642.1:c.705T>C	ENSP00000501242.1:p.His235=
ENST00000673991.1:c.1082T>C	ENSP00000501033.1:p.Ile361Thr
ENST00000226760.5:c.1046T>C MANE Select	ENSP00000226760.1:p.Ile349Thr
ENST00000503569.5:c.1046T>C	ENSP00000423337.1:p.Ile349Thr
ENST00000506362.1:c.679T>C
ENST00000507765.1:n.1231T>C
NM_001145853.1:c.1046T>C	NP_001139325.1:p.Ile349Thr
NM_006005.3:c.1046T>C MANE Select	NP_005996.2:p.Ile349Thr
XM_017008586.1:c.1055T>C	XP_016864075.1:p.Ile352Thr