Canonical Allele Identifier: CA1435772029

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300710C= , CM000666.2:g.6300710C=	GRCh38
NC_000004.11:g.6302437C= , CM000666.1:g.6302437C=	GRCh37
NC_000004.10:g.6353338C=	NCBI36
NG_011700.1:g.35861C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.951C=	ENSP00000507852.1:p.Asp317=
ENST00000683395.1:c.892C=
ENST00000684087.1:c.915C=	ENSP00000506978.1:p.Asp305=
ENST00000506362.2:c.666C=	ENSP00000424103.2:p.Asp222=
ENST00000673642.1:c.661-87C=	ENSP00000501242.1:n.661-87C=
ENST00000673991.1:c.951C=	ENSP00000501033.1:p.Asp317=
ENST00000226760.5:c.915C= MANE Select	ENSP00000226760.1:p.Asp305=
ENST00000503569.5:c.915C=	ENSP00000423337.1:p.Asp305=
ENST00000506362.1:c.548C=
ENST00000507765.1:n.1100C=
ENST00000513395.1:n.473C=
NM_001145853.1:c.915C=	NP_001139325.1:p.Asp305=
NM_006005.3:c.915C= MANE Select	NP_005996.2:p.Asp305=
XM_017008586.1:c.924C=	XP_016864075.1:p.Asp308=