Canonical Allele Identifier: CA356178490

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6303912A>G (hg19) ; chr4:g.6302185A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302185A>G , CM000666.2:g.6302185A>G	GRCh38
NC_000004.11:g.6303912A>G , CM000666.1:g.6303912A>G	GRCh37
NC_000004.10:g.6354813A>G	NCBI36
NG_011700.1:g.37336A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.2426A>G	ENSP00000507852.1:p.Asp809Gly
ENST00000683395.1:c.2367A>G
ENST00000684087.1:c.2390A>G	ENSP00000506978.1:p.Asp797Gly
ENST00000506362.2:c.2141A>G	ENSP00000424103.2:p.Asp714Gly
ENST00000673991.1:c.2426A>G	ENSP00000501033.1:p.Asp809Gly
ENST00000226760.5:c.2390A>G MANE Select	ENSP00000226760.1:p.Asp797Gly
ENST00000503569.5:c.2390A>G	ENSP00000423337.1:p.Asp797Gly
ENST00000507765.1:n.2575A>G
NM_001145853.1:c.2390A>G	NP_001139325.1:p.Asp797Gly
NM_006005.3:c.2390A>G MANE Select	NP_005996.2:p.Asp797Gly
XM_017008586.1:c.2399A>G	XP_016864075.1:p.Asp800Gly