Canonical Allele Identifier: CA645523669

Gene: WFS1

Linked Data

• COSMIC: COSM4516228

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301502_6301503delinsTT , CM000666.2:g.6301502_6301503delinsTT	GRCh38
NC_000004.11:g.6303229_6303230delinsTT , CM000666.1:g.6303229_6303230delinsTT	GRCh37
NC_000004.10:g.6354130_6354131delinsTT	NCBI36
NG_011700.1:g.36653_36654delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1743_1744delinsTT	ENSP00000507852.1:p.Leu582Phe
ENST00000683395.1:c.1684_1685delinsTT
ENST00000684087.1:c.1707_1708delinsTT	ENSP00000506978.1:p.Leu570Phe
ENST00000506362.2:c.1458_1459delinsTT	ENSP00000424103.2:p.Leu487Phe
ENST00000673642.1:c.1366_1367delinsTT	ENSP00000501242.1:n.1366_1367delinsTT
ENST00000673991.1:c.1743_1744delinsTT	ENSP00000501033.1:p.Leu582Phe
ENST00000226760.5:c.1707_1708delinsTT MANE Select	ENSP00000226760.1:p.Leu570Phe
ENST00000503569.5:c.1707_1708delinsTT	ENSP00000423337.1:p.Leu570Phe
ENST00000507765.1:n.1892_1893delinsTT
NM_001145853.1:c.1707_1708delinsTT	NP_001139325.1:p.Leu570Phe
NM_006005.3:c.1707_1708delinsTT MANE Select	NP_005996.2:p.Leu570Phe
XM_017008586.1:c.1716_1717delinsTT	XP_016864075.1:p.Leu573Phe