Canonical Allele Identifier: CA1435772323

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300877C= , CM000666.2:g.6300877C=	GRCh38
NC_000004.11:g.6302604C= , CM000666.1:g.6302604C=	GRCh37
NC_000004.10:g.6353505C=	NCBI36
NG_011700.1:g.36028C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1118C=	ENSP00000507852.1:p.Thr373=
ENST00000683395.1:c.1059C=
ENST00000684087.1:c.1082C=	ENSP00000506978.1:p.Thr361=
ENST00000506362.2:c.833C=	ENSP00000424103.2:p.Thr278=
ENST00000673642.1:c.741C=	ENSP00000501242.1:p.His247=
ENST00000673991.1:c.1118C=	ENSP00000501033.1:p.Thr373=
ENST00000226760.5:c.1082C= MANE Select	ENSP00000226760.1:p.Thr361=
ENST00000503569.5:c.1082C=	ENSP00000423337.1:p.Thr361=
ENST00000506362.1:c.715C=
ENST00000507765.1:n.1267C=
NM_001145853.1:c.1082C=	NP_001139325.1:p.Thr361=
NM_006005.3:c.1082C= MANE Select	NP_005996.2:p.Thr361=
XM_017008586.1:c.1091C=	XP_016864075.1:p.Thr364=