Canonical Allele Identifier: CA356176952

Gene: WFS1

Linked Data

• ClinVar Variation Id: 2794567
• ClinVar RCV Id: RCV003672922
• dbSNP Id: rs553336498
• MyVariant Identifiers: chr4:g.6303368G>C (hg19) ; chr4:g.6301641G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301641G>C , CM000666.2:g.6301641G>C	GRCh38
NC_000004.11:g.6303368G>C , CM000666.1:g.6303368G>C	GRCh37
NC_000004.10:g.6354269G>C	NCBI36
NG_011700.1:g.36792G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.1882G>C	ENSP00000507852.1:p.Ala628Pro
ENST00000683395.1:c.1823G>C
ENST00000684087.1:c.1846G>C	ENSP00000506978.1:p.Ala616Pro
ENST00000506362.2:c.1597G>C	ENSP00000424103.2:p.Ala533Pro
ENST00000673642.1:c.1505G>C	ENSP00000501242.1:n.1505G>C
ENST00000673991.1:c.1882G>C	ENSP00000501033.1:p.Ala628Pro
ENST00000226760.5:c.1846G>C MANE Select	ENSP00000226760.1:p.Ala616Pro
ENST00000503569.5:c.1846G>C	ENSP00000423337.1:p.Ala616Pro
ENST00000507765.1:n.2031G>C
NM_001145853.1:c.1846G>C	NP_001139325.1:p.Ala616Pro
NM_006005.3:c.1846G>C MANE Select	NP_005996.2:p.Ala616Pro
XM_017008586.1:c.1855G>C	XP_016864075.1:p.Ala619Pro