Canonical Allele Identifier: CA1435768975

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291971T= , CM000666.2:g.6291971T=	GRCh38
NC_000004.11:g.6293698T= , CM000666.1:g.6293698T=	GRCh37
NC_000004.10:g.6344599T=	NCBI36
NG_011700.1:g.27122T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.686T=	ENSP00000507852.1:p.Met229=
ENST00000683395.1:c.663T=
ENST00000684087.1:c.686T=	ENSP00000506978.1:p.Met229=
ENST00000506362.2:c.437T=	ENSP00000424103.2:p.Met146=
ENST00000673642.1:c.485T=	ENSP00000501242.1:p.Met162=
ENST00000673991.1:c.686T=	ENSP00000501033.1:p.Met229=
ENST00000226760.5:c.686T= MANE Select	ENSP00000226760.1:p.Met229=
ENST00000503569.5:c.686T=	ENSP00000423337.1:p.Met229=
ENST00000506362.1:c.283T=
ENST00000507765.1:n.871T=
NM_001145853.1:c.686T=	NP_001139325.1:p.Met229=
NM_006005.3:c.686T= MANE Select	NP_005996.2:p.Met229=
XM_017008586.1:c.695T=	XP_016864075.1:p.Met232=