Canonical Allele Identifier: CA356179256

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6304089C>A (hg19) ; chr4:g.6302362C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302362C>A , CM000666.2:g.6302362C>A	GRCh38
NC_000004.11:g.6304089C>A , CM000666.1:g.6304089C>A	GRCh37
NC_000004.10:g.6354990C>A	NCBI36
NG_011700.1:g.37513C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2603C>A	ENSP00000507852.1:p.Pro868His
ENST00000683395.1:c.2544C>A
ENST00000684087.1:c.2567C>A	ENSP00000506978.1:p.Pro856His
ENST00000506362.2:c.2318C>A	ENSP00000424103.2:p.Pro773His
ENST00000673991.1:c.2603C>A	ENSP00000501033.1:p.Pro868His
ENST00000226760.5:c.2567C>A MANE Select	ENSP00000226760.1:p.Pro856His
ENST00000503569.5:c.2567C>A	ENSP00000423337.1:p.Pro856His
ENST00000507765.1:n.2752C>A
NM_001145853.1:c.2567C>A	NP_001139325.1:p.Pro856His
NM_006005.3:c.2567C>A MANE Select	NP_005996.2:p.Pro856His
XM_017008586.1:c.2576C>A	XP_016864075.1:p.Pro859His