Canonical Allele Identifier: CA1435771933

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300664A= , CM000666.2:g.6300664A=	GRCh38
NC_000004.11:g.6302391A= , CM000666.1:g.6302391A=	GRCh37
NC_000004.10:g.6353292A=	NCBI36
NG_011700.1:g.35815A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.905A=	ENSP00000507852.1:p.Lys302=
ENST00000683395.1:c.846A=
ENST00000684087.1:c.869A=	ENSP00000506978.1:p.Lys290=
ENST00000506362.2:c.620A=	ENSP00000424103.2:p.Lys207=
ENST00000673642.1:c.661-133A=	ENSP00000501242.1:n.661-133A=
ENST00000673991.1:c.905A=	ENSP00000501033.1:p.Lys302=
ENST00000226760.5:c.869A= MANE Select	ENSP00000226760.1:p.Lys290=
ENST00000503569.5:c.869A=	ENSP00000423337.1:p.Lys290=
ENST00000506362.1:c.502A=
ENST00000507765.1:n.1054A=
ENST00000513395.1:n.427A=
NM_001145853.1:c.869A=	NP_001139325.1:p.Lys290=
NM_006005.3:c.869A= MANE Select	NP_005996.2:p.Lys290=
XM_017008586.1:c.878A=	XP_016864075.1:p.Lys293=