Canonical Allele Identifier: CA356176514

Gene: WFS1

Linked Data

• dbSNP Id: rs1560419855
• gnomAD v3: 4-6301480-G-A
• gnomAD v4: 4-6301480-G-A
• MyVariant Identifiers: chr4:g.6303207G>A (hg19) ; chr4:g.6301480G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301480G>A , CM000666.2:g.6301480G>A	GRCh38
NC_000004.11:g.6303207G>A , CM000666.1:g.6303207G>A	GRCh37
NC_000004.10:g.6354108G>A	NCBI36
NG_011700.1:g.36631G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1721G>A	ENSP00000507852.1:p.Gly574Asp
ENST00000683395.1:c.1662G>A
ENST00000684087.1:c.1685G>A	ENSP00000506978.1:p.Gly562Asp
ENST00000506362.2:c.1436G>A	ENSP00000424103.2:p.Gly479Asp
ENST00000673642.1:c.1344G>A	ENSP00000501242.1:n.1344G>A
ENST00000673991.1:c.1721G>A	ENSP00000501033.1:p.Gly574Asp
ENST00000226760.5:c.1685G>A MANE Select	ENSP00000226760.1:p.Gly562Asp
ENST00000503569.5:c.1685G>A	ENSP00000423337.1:p.Gly562Asp
ENST00000507765.1:n.1870G>A
NM_001145853.1:c.1685G>A	NP_001139325.1:p.Gly562Asp
NM_006005.3:c.1685G>A MANE Select	NP_005996.2:p.Gly562Asp
XM_017008586.1:c.1694G>A	XP_016864075.1:p.Gly565Asp