Canonical Allele Identifier: CA356177632

Gene: WFS1

Linked Data

• dbSNP Id: rs1197749524
• gnomAD v2: 4-6303588-T-C
• gnomAD v4: 4-6301861-T-C
• MyVariant Identifiers: chr4:g.6303588T>C (hg19) ; chr4:g.6301861T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301861T>C , CM000666.2:g.6301861T>C	GRCh38
NC_000004.11:g.6303588T>C , CM000666.1:g.6303588T>C	GRCh37
NC_000004.10:g.6354489T>C	NCBI36
NG_011700.1:g.37012T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2102T>C	ENSP00000507852.1:p.Leu701Pro
ENST00000683395.1:c.2043T>C
ENST00000684087.1:c.2066T>C	ENSP00000506978.1:p.Leu689Pro
ENST00000506362.2:c.1817T>C	ENSP00000424103.2:p.Leu606Pro
ENST00000673642.1:c.1725T>C	ENSP00000501242.1:n.1725T>C
ENST00000673991.1:c.2102T>C	ENSP00000501033.1:p.Leu701Pro
ENST00000226760.5:c.2066T>C MANE Select	ENSP00000226760.1:p.Leu689Pro
ENST00000503569.5:c.2066T>C	ENSP00000423337.1:p.Leu689Pro
ENST00000507765.1:n.2251T>C
NM_001145853.1:c.2066T>C	NP_001139325.1:p.Leu689Pro
NM_006005.3:c.2066T>C MANE Select	NP_005996.2:p.Leu689Pro
XM_017008586.1:c.2075T>C	XP_016864075.1:p.Leu692Pro