Canonical Allele Identifier: CA2760284128

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291598_6291599insAG , CM000666.2:g.6291598_6291599insAG	GRCh38
NC_000004.11:g.6293325_6293326insAG , CM000666.1:g.6293325_6293326insAG	GRCh37
NC_000004.10:g.6344226_6344227insAG	NCBI36
NG_011700.1:g.26749_26750insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+231_631+232insAG	ENSP00000507852.1:n.631+231_631+232insAG
ENST00000683395.1:c.608+244_608+245insAG
ENST00000684087.1:c.631+231_631+232insAG	ENSP00000506978.1:n.631+231_631+232insAG
ENST00000684700.1:c.*157_*158insAG	ENSP00000507806.1:n.*157_*158insAG
ENST00000506362.2:c.382+231_382+232insAG	ENSP00000424103.2:n.382+231_382+232insAG
ENST00000673642.1:c.430+231_430+232insAG	ENSP00000501242.1:n.430+231_430+232insAG
ENST00000673991.1:c.631+231_631+232insAG	ENSP00000501033.1:n.631+231_631+232insAG
ENST00000226760.5:c.631+231_631+232insAG MANE Select	ENSP00000226760.1:n.631+231_631+232insAG
ENST00000503569.5:c.631+231_631+232insAG	ENSP00000423337.1:n.631+231_631+232insAG
ENST00000506362.1:c.228+231_228+232insAG
ENST00000507765.1:n.816+231_816+232insAG
NM_001145853.1:c.631+231_631+232insAG	NP_001139325.1:n.631+231_631+232insAG
NM_006005.3:c.631+231_631+232insAG MANE Select	NP_005996.2:n.631+231_631+232insAG
XM_017008586.1:c.640+231_640+232insAG	XP_016864075.1:n.640+231_640+232insAG