Canonical Allele Identifier: CA1435771666

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300444G= , CM000666.2:g.6300444G=	GRCh38
NC_000004.11:g.6302171G= , CM000666.1:g.6302171G=	GRCh37
NC_000004.10:g.6353072G=	NCBI36
NG_011700.1:g.35595G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-213G=	ENSP00000507852.1:n.898-213G=
ENST00000683395.1:c.839-213G=
ENST00000684087.1:c.862-213G=	ENSP00000506978.1:n.862-213G=
ENST00000506362.2:c.613-213G=	ENSP00000424103.2:n.613-213G=
ENST00000673642.1:c.661-353G=	ENSP00000501242.1:n.661-353G=
ENST00000673991.1:c.898-213G=	ENSP00000501033.1:n.898-213G=
ENST00000226760.5:c.862-213G= MANE Select	ENSP00000226760.1:n.862-213G=
ENST00000503569.5:c.862-213G=	ENSP00000423337.1:n.862-213G=
ENST00000506362.1:c.495-213G=
ENST00000507765.1:n.1047-213G=
ENST00000513395.1:n.420-213G=
NM_001145853.1:c.862-213G=	NP_001139325.1:n.862-213G=
NM_006005.3:c.862-213G= MANE Select	NP_005996.2:n.862-213G=
XM_017008586.1:c.871-213G=	XP_016864075.1:n.871-213G=