Canonical Allele Identifier: CA1435773321

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302895_6302899delinsCTTAT , CM000666.2:g.6302895_6302899delinsCTTAT	GRCh38
NC_000004.11:g.6304622_6304626delinsCTTAT , CM000666.1:g.6304622_6304626delinsCTTAT	GRCh37
NC_000004.10:g.6355523_6355527delinsCTTAT	NCBI36
NG_011700.1:g.38046_38050delinsCTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*427_*431delinsCTTAT	ENSP00000507852.1:n.*427_*431delinsCTTAT
ENST00000683395.1:c.3077_3081delinsCTTAT
ENST00000684087.1:c.*427_*431delinsCTTAT	ENSP00000506978.1:n.*427_*431delinsCTTAT
ENST00000673991.1:c.*427_*431delinsCTTAT	ENSP00000501033.1:n.*427_*431delinsCTTAT
ENST00000226760.5:c.*427_*431delinsCTTAT MANE Select	ENSP00000226760.1:n.*427_*431delinsCTTAT
ENST00000507765.1:n.3285_3289delinsCTTAT
NM_001145853.1:c.*427_*431delinsCTTAT	NP_001139325.1:n.*427_*431delinsCTTAT
NM_006005.3:c.*427_*431delinsCTTAT MANE Select	NP_005996.2:n.*427_*431delinsCTTAT
XM_017008586.1:c.*427_*431delinsCTTAT	XP_016864075.1:n.*427_*431delinsCTTAT
XR_001741566.2:n.2046_2050delinsATAAG