Canonical Allele Identifier: CA2760284046

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291542_6291543insAG , CM000666.2:g.6291542_6291543insAG	GRCh38
NC_000004.11:g.6293269_6293270insAG , CM000666.1:g.6293269_6293270insAG	GRCh37
NC_000004.10:g.6344170_6344171insAG	NCBI36
NG_011700.1:g.26693_26694insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+175_631+176insAG	ENSP00000507852.1:n.631+175_631+176insAG
ENST00000683395.1:c.608+188_608+189insAG
ENST00000684087.1:c.631+175_631+176insAG	ENSP00000506978.1:n.631+175_631+176insAG
ENST00000684700.1:c.*101_*102insAG	ENSP00000507806.1:n.*101_*102insAG
ENST00000506362.2:c.382+175_382+176insAG	ENSP00000424103.2:n.382+175_382+176insAG
ENST00000673642.1:c.430+175_430+176insAG	ENSP00000501242.1:n.430+175_430+176insAG
ENST00000673991.1:c.631+175_631+176insAG	ENSP00000501033.1:n.631+175_631+176insAG
ENST00000226760.5:c.631+175_631+176insAG MANE Select	ENSP00000226760.1:n.631+175_631+176insAG
ENST00000503569.5:c.631+175_631+176insAG	ENSP00000423337.1:n.631+175_631+176insAG
ENST00000506362.1:c.228+175_228+176insAG
ENST00000507765.1:n.816+175_816+176insAG
NM_001145853.1:c.631+175_631+176insAG	NP_001139325.1:n.631+175_631+176insAG
NM_006005.3:c.631+175_631+176insAG MANE Select	NP_005996.2:n.631+175_631+176insAG
XM_017008586.1:c.640+175_640+176insAG	XP_016864075.1:n.640+175_640+176insAG