Canonical Allele Identifier: CA1435773235

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302822_6302830delinsCCTCTTTCT , CM000666.2:g.6302822_6302830delinsCCTCTTTCT	GRCh38
NC_000004.11:g.6304549_6304557delinsCCTCTTTCT , CM000666.1:g.6304549_6304557delinsCCTCTTTCT	GRCh37
NC_000004.10:g.6355450_6355458delinsCCTCTTTCT	NCBI36
NG_011700.1:g.37973_37981delinsCCTCTTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*354_*362delinsCCTCTTTCT	ENSP00000507852.1:n.*354_*362delinsCCTCTTTCT
ENST00000683395.1:c.3004_3012delinsCCTCTTTCT
ENST00000684087.1:c.*354_*362delinsCCTCTTTCT	ENSP00000506978.1:n.*354_*362delinsCCTCTTTCT
ENST00000506362.2:c.*354_*362delinsCCTCTTTCT	ENSP00000424103.2:n.*354_*362delinsCCTCTTTCT
ENST00000673991.1:c.*354_*362delinsCCTCTTTCT	ENSP00000501033.1:n.*354_*362delinsCCTCTTTCT
ENST00000226760.5:c.*354_*362delinsCCTCTTTCT MANE Select	ENSP00000226760.1:n.*354_*362delinsCCTCTTTCT
ENST00000503569.5:c.*354_*362delinsCCTCTTTCT	ENSP00000423337.1:n.*354_*362delinsCCTCTTTCT
ENST00000507765.1:n.3212_3220delinsCCTCTTTCT
NM_001145853.1:c.*354_*362delinsCCTCTTTCT	NP_001139325.1:n.*354_*362delinsCCTCTTTCT
NM_006005.3:c.*354_*362delinsCCTCTTTCT MANE Select	NP_005996.2:n.*354_*362delinsCCTCTTTCT
XM_017008586.1:c.*354_*362delinsCCTCTTTCT	XP_016864075.1:n.*354_*362delinsCCTCTTTCT