Canonical Allele Identifier: CA438368272

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6303883T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302156T>G , CM000666.2:g.6302156T>G	GRCh38
NC_000004.11:g.6303883T>G , CM000666.1:g.6303883T>G	GRCh37
NC_000004.10:g.6354784T>G	NCBI36
NG_011700.1:g.37307T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2397T>G	ENSP00000507852.1:p.Ala799=
ENST00000683395.1:c.2338T>G
ENST00000684087.1:c.2361T>G	ENSP00000506978.1:p.Ala787=
ENST00000506362.2:c.2112T>G	ENSP00000424103.2:p.Ala704=
ENST00000673991.1:c.2397T>G	ENSP00000501033.1:p.Ala799=
ENST00000226760.5:c.2361T>G MANE Select	ENSP00000226760.1:p.Ala787=
ENST00000503569.5:c.2361T>G	ENSP00000423337.1:p.Ala787=
ENST00000507765.1:n.2546T>G
NM_001145853.1:c.2361T>G	NP_001139325.1:p.Ala787=
NM_006005.3:c.2361T>G MANE Select	NP_005996.2:p.Ala787=
XM_017008586.1:c.2370T>G	XP_016864075.1:p.Ala790=