Canonical Allele Identifier: CA797211921

Gene: WFS1

Linked Data

• dbSNP Id: rs960533920
• gnomAD v3: 4-6302671-A-C
• gnomAD v4: 4-6302671-A-C
• MyVariant Identifiers: chr4:g.6304398A>C (hg19) ; chr4:g.6302671A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302671A>C , CM000666.2:g.6302671A>C	GRCh38
NC_000004.11:g.6304398A>C , CM000666.1:g.6304398A>C	GRCh37
NC_000004.10:g.6355299A>C	NCBI36
NG_011700.1:g.37822A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*203A>C	ENSP00000507852.1:n.*203A>C
ENST00000683395.1:c.2853A>C
ENST00000684087.1:c.*203A>C	ENSP00000506978.1:n.*203A>C
ENST00000506362.2:c.*203A>C	ENSP00000424103.2:n.*203A>C
ENST00000673991.1:c.*203A>C	ENSP00000501033.1:n.*203A>C
ENST00000226760.5:c.*203A>C MANE Select	ENSP00000226760.1:n.*203A>C
ENST00000503569.5:c.*203A>C	ENSP00000423337.1:n.*203A>C
ENST00000507765.1:n.3061A>C
NM_001145853.1:c.*203A>C	NP_001139325.1:n.*203A>C
NM_006005.3:c.*203A>C MANE Select	NP_005996.2:n.*203A>C
XM_017008586.1:c.*203A>C	XP_016864075.1:n.*203A>C