Canonical Allele Identifier: CA438368532

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6303073C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301346C>G , CM000666.2:g.6301346C>G	GRCh38
NC_000004.11:g.6303073C>G , CM000666.1:g.6303073C>G	GRCh37
NC_000004.10:g.6353974C>G	NCBI36
NG_011700.1:g.36497C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1587C>G	ENSP00000507852.1:p.Arg529=
ENST00000683395.1:c.1528C>G
ENST00000684087.1:c.1551C>G	ENSP00000506978.1:p.Arg517=
ENST00000506362.2:c.1302C>G	ENSP00000424103.2:p.Arg434=
ENST00000673642.1:c.1210C>G	ENSP00000501242.1:p.His404Asp
ENST00000673991.1:c.1587C>G	ENSP00000501033.1:p.Arg529=
ENST00000226760.5:c.1551C>G MANE Select	ENSP00000226760.1:p.Arg517=
ENST00000503569.5:c.1551C>G	ENSP00000423337.1:p.Arg517=
ENST00000507765.1:n.1736C>G
NM_001145853.1:c.1551C>G	NP_001139325.1:p.Arg517=
NM_006005.3:c.1551C>G MANE Select	NP_005996.2:p.Arg517=
XM_017008586.1:c.1560C>G	XP_016864075.1:p.Arg520=