Canonical Allele Identifier: CA2501554402

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291475_6291476insAG , CM000666.2:g.6291475_6291476insAG	GRCh38
NC_000004.11:g.6293202_6293203insAG , CM000666.1:g.6293202_6293203insAG	GRCh37
NC_000004.10:g.6344103_6344104insAG	NCBI36
NG_011700.1:g.26626_26627insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+108_631+109insAG	ENSP00000507852.1:n.631+108_631+109insAG
ENST00000683395.1:c.608+121_608+122insAG
ENST00000684087.1:c.631+108_631+109insAG	ENSP00000506978.1:n.631+108_631+109insAG
ENST00000684700.1:c.*34_*35insAG	ENSP00000507806.1:n.*34_*35insAG
ENST00000506362.2:c.382+108_382+109insAG	ENSP00000424103.2:n.382+108_382+109insAG
ENST00000673642.1:c.430+108_430+109insAG	ENSP00000501242.1:n.430+108_430+109insAG
ENST00000673991.1:c.631+108_631+109insAG	ENSP00000501033.1:n.631+108_631+109insAG
ENST00000226760.5:c.631+108_631+109insAG MANE Select	ENSP00000226760.1:n.631+108_631+109insAG
ENST00000503569.5:c.631+108_631+109insAG	ENSP00000423337.1:n.631+108_631+109insAG
ENST00000506362.1:c.228+108_228+109insAG
ENST00000507765.1:n.816+108_816+109insAG
NM_001145853.1:c.631+108_631+109insAG	NP_001139325.1:n.631+108_631+109insAG
NM_006005.3:c.631+108_631+109insAG MANE Select	NP_005996.2:n.631+108_631+109insAG
XM_017008586.1:c.640+108_640+109insAG	XP_016864075.1:n.640+108_640+109insAG