Canonical Allele Identifier: CA2669843857

Gene: WFS1

Linked Data

• gnomAD v4: 4-6302794-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302794T>C , CM000666.2:g.6302794T>C	GRCh38
NC_000004.11:g.6304521T>C , CM000666.1:g.6304521T>C	GRCh37
NC_000004.10:g.6355422T>C	NCBI36
NG_011700.1:g.37945T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*326T>C	ENSP00000507852.1:n.*326T>C
ENST00000683395.1:c.2976T>C
ENST00000684087.1:c.*326T>C	ENSP00000506978.1:n.*326T>C
ENST00000506362.2:c.*326T>C	ENSP00000424103.2:n.*326T>C
ENST00000673991.1:c.*326T>C	ENSP00000501033.1:n.*326T>C
ENST00000226760.5:c.*326T>C MANE Select	ENSP00000226760.1:n.*326T>C
ENST00000503569.5:c.*326T>C	ENSP00000423337.1:n.*326T>C
ENST00000507765.1:n.3184T>C
NM_001145853.1:c.*326T>C	NP_001139325.1:n.*326T>C
NM_006005.3:c.*326T>C MANE Select	NP_005996.2:n.*326T>C
XM_017008586.1:c.*326T>C	XP_016864075.1:n.*326T>C