Canonical Allele Identifier: CA2760284002

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291515_6291516insA , CM000666.2:g.6291515_6291516insA	GRCh38
NC_000004.11:g.6293242_6293243insA , CM000666.1:g.6293242_6293243insA	GRCh37
NC_000004.10:g.6344143_6344144insA	NCBI36
NG_011700.1:g.26666_26667insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+148_631+149insA	ENSP00000507852.1:n.631+148_631+149insA
ENST00000683395.1:c.608+161_608+162insA
ENST00000684087.1:c.631+148_631+149insA	ENSP00000506978.1:n.631+148_631+149insA
ENST00000684700.1:c.*74_*75insA	ENSP00000507806.1:n.*74_*75insA
ENST00000506362.2:c.382+148_382+149insA	ENSP00000424103.2:n.382+148_382+149insA
ENST00000673642.1:c.430+148_430+149insA	ENSP00000501242.1:n.430+148_430+149insA
ENST00000673991.1:c.631+148_631+149insA	ENSP00000501033.1:n.631+148_631+149insA
ENST00000226760.5:c.631+148_631+149insA MANE Select	ENSP00000226760.1:n.631+148_631+149insA
ENST00000503569.5:c.631+148_631+149insA	ENSP00000423337.1:n.631+148_631+149insA
ENST00000506362.1:c.228+148_228+149insA
ENST00000507765.1:n.816+148_816+149insA
NM_001145853.1:c.631+148_631+149insA	NP_001139325.1:n.631+148_631+149insA
NM_006005.3:c.631+148_631+149insA MANE Select	NP_005996.2:n.631+148_631+149insA
XM_017008586.1:c.640+148_640+149insA	XP_016864075.1:n.640+148_640+149insA