Canonical Allele Identifier: CA1435772683

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302366C= , CM000666.2:g.6302366C=	GRCh38
NC_000004.11:g.6304093C= , CM000666.1:g.6304093C=	GRCh37
NC_000004.10:g.6354994C=	NCBI36
NG_011700.1:g.37517C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2607C=	ENSP00000507852.1:p.Thr869=
ENST00000683395.1:c.2548C=
ENST00000684087.1:c.2571C=	ENSP00000506978.1:p.Thr857=
ENST00000506362.2:c.2322C=	ENSP00000424103.2:p.Thr774=
ENST00000673991.1:c.2607C=	ENSP00000501033.1:p.Thr869=
ENST00000226760.5:c.2571C= MANE Select	ENSP00000226760.1:p.Thr857=
ENST00000503569.5:c.2571C=	ENSP00000423337.1:p.Thr857=
ENST00000507765.1:n.2756C=
NM_001145853.1:c.2571C=	NP_001139325.1:p.Thr857=
NM_006005.3:c.2571C= MANE Select	NP_005996.2:p.Thr857=
XM_017008586.1:c.2580C=	XP_016864075.1:p.Thr860=