Canonical Allele Identifier: CA1435768802

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291654C= , CM000666.2:g.6291654C=	GRCh38
NC_000004.11:g.6293381C= , CM000666.1:g.6293381C=	GRCh37
NC_000004.10:g.6344282C=	NCBI36
NG_011700.1:g.26805C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.632-263C=	ENSP00000507852.1:n.632-263C=
ENST00000683395.1:c.609-263C=
ENST00000684087.1:c.632-263C=	ENSP00000506978.1:n.632-263C=
ENST00000506362.2:c.383-263C=	ENSP00000424103.2:n.383-263C=
ENST00000673642.1:c.431-263C=	ENSP00000501242.1:n.431-263C=
ENST00000673991.1:c.632-263C=	ENSP00000501033.1:n.632-263C=
ENST00000226760.5:c.632-263C= MANE Select	ENSP00000226760.1:n.632-263C=
ENST00000503569.5:c.632-263C=	ENSP00000423337.1:n.632-263C=
ENST00000506362.1:c.229-263C=
ENST00000507765.1:n.817-263C=
NM_001145853.1:c.632-263C=	NP_001139325.1:n.632-263C=
NM_006005.3:c.632-263C= MANE Select	NP_005996.2:n.632-263C=
XM_017008586.1:c.641-263C=	XP_016864075.1:n.641-263C=