Canonical Allele Identifier: CA356179849

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6304191C>A (hg19) ; chr4:g.6302464C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302464C>A , CM000666.2:g.6302464C>A	GRCh38
NC_000004.11:g.6304191C>A , CM000666.1:g.6304191C>A	GRCh37
NC_000004.10:g.6355092C>A	NCBI36
NG_011700.1:g.37615C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2705C>A	ENSP00000507852.1:p.Ala902Asp
ENST00000683395.1:c.2646C>A
ENST00000684087.1:c.2669C>A	ENSP00000506978.1:p.Ala890Asp
ENST00000506362.2:c.2420C>A	ENSP00000424103.2:p.Ala807Asp
ENST00000673991.1:c.2705C>A	ENSP00000501033.1:p.Ala902Asp
ENST00000226760.5:c.2669C>A MANE Select	ENSP00000226760.1:p.Ala890Asp
ENST00000503569.5:c.2669C>A	ENSP00000423337.1:p.Ala890Asp
ENST00000507765.1:n.2854C>A
NM_001145853.1:c.2669C>A	NP_001139325.1:p.Ala890Asp
NM_006005.3:c.2669C>A MANE Select	NP_005996.2:p.Ala890Asp
XM_017008586.1:c.2678C>A	XP_016864075.1:p.Ala893Asp