Canonical Allele Identifier: CA1435768572

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291213C= , CM000666.2:g.6291213C=	GRCh38
NC_000004.11:g.6292940C= , CM000666.1:g.6292940C=	GRCh37
NC_000004.10:g.6343841C=	NCBI36
NG_011700.1:g.26364C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.477C=	ENSP00000507852.1:p.Asn159=
ENST00000683395.1:c.467C=
ENST00000684087.1:c.477C=	ENSP00000506978.1:p.Asn159=
ENST00000684700.1:c.477C=	ENSP00000507806.1:p.Asn159=
ENST00000506362.2:c.228C=	ENSP00000424103.2:p.Asn76=
ENST00000673642.1:c.276C=	ENSP00000501242.1:p.Asn92=
ENST00000673991.1:c.477C=	ENSP00000501033.1:p.Asn159=
ENST00000674051.1:c.351C=	ENSP00000501083.1:p.Asn117=
ENST00000226760.5:c.477C= MANE Select	ENSP00000226760.1:p.Asn159=
ENST00000503569.5:c.477C=	ENSP00000423337.1:p.Asn159=
ENST00000506362.1:c.74C=
ENST00000507765.1:n.662C=
NM_001145853.1:c.477C=	NP_001139325.1:p.Asn159=
NM_006005.3:c.477C= MANE Select	NP_005996.2:p.Asn159=
XM_017008586.1:c.486C=	XP_016864075.1:p.Asn162=