Canonical Allele Identifier: CA1435768789

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291623T= , CM000666.2:g.6291623T=	GRCh38
NC_000004.11:g.6293350T= , CM000666.1:g.6293350T=	GRCh37
NC_000004.10:g.6344251T=	NCBI36
NG_011700.1:g.26774T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.631+256T=	ENSP00000507852.1:n.631+256T=
ENST00000683395.1:c.608+269T=
ENST00000684087.1:c.631+256T=	ENSP00000506978.1:n.631+256T=
ENST00000684700.1:c.*182T=	ENSP00000507806.1:n.*182T=
ENST00000506362.2:c.382+256T=	ENSP00000424103.2:n.382+256T=
ENST00000673642.1:c.430+256T=	ENSP00000501242.1:n.430+256T=
ENST00000673991.1:c.631+256T=	ENSP00000501033.1:n.631+256T=
ENST00000226760.5:c.631+256T= MANE Select	ENSP00000226760.1:n.631+256T=
ENST00000503569.5:c.631+256T=	ENSP00000423337.1:n.631+256T=
ENST00000506362.1:c.228+256T=
ENST00000507765.1:n.816+256T=
NM_001145853.1:c.631+256T=	NP_001139325.1:n.631+256T=
NM_006005.3:c.631+256T= MANE Select	NP_005996.2:n.631+256T=
XM_017008586.1:c.640+256T=	XP_016864075.1:n.640+256T=