Canonical Allele Identifier: CA1435768947

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291926C= , CM000666.2:g.6291926C=	GRCh38
NC_000004.11:g.6293653C= , CM000666.1:g.6293653C=	GRCh37
NC_000004.10:g.6344554C=	NCBI36
NG_011700.1:g.27077C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.641C=	ENSP00000507852.1:p.Ala214=
ENST00000683395.1:c.618C=
ENST00000684087.1:c.641C=	ENSP00000506978.1:p.Ala214=
ENST00000506362.2:c.392C=	ENSP00000424103.2:p.Ala131=
ENST00000673642.1:c.440C=	ENSP00000501242.1:p.Ala147=
ENST00000673991.1:c.641C=	ENSP00000501033.1:p.Ala214=
ENST00000226760.5:c.641C= MANE Select	ENSP00000226760.1:p.Ala214=
ENST00000503569.5:c.641C=	ENSP00000423337.1:p.Ala214=
ENST00000506362.1:c.238C=
ENST00000507765.1:n.826C=
NM_001145853.1:c.641C=	NP_001139325.1:p.Ala214=
NM_006005.3:c.641C= MANE Select	NP_005996.2:p.Ala214=
XM_017008586.1:c.650C=	XP_016864075.1:p.Ala217=