Canonical Allele Identifier: CA1926177472

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967895_87967899delinsCCTTA , CM000672.2:g.87967895_87967899delinsCCTTA	GRCh38
NC_000010.10:g.89727652_89727656delinsCCTTA , CM000672.1:g.89727652_89727656delinsCCTTA	GRCh37
NC_000010.9:g.89717632_89717636delinsCCTTA	NCBI36
NG_007466.2:g.109457_109461delinsCCTTA , LRG_311:g.109457_109461delinsCCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2664_*2668delinsCCTTA	ENSP00000518161.1:n.*2664_*2668delinsCCTTA
ENST00000688158.2:n.4370_4374delinsCCTTA
ENST00000706954.1:c.*2423_*2427delinsCCTTA	ENSP00000516674.1:n.*2423_*2427delinsCCTTA
ENST00000706955.1:c.*3670_*3674delinsCCTTA	ENSP00000516675.1:n.*3670_*3674delinsCCTTA
ENST00000688158.1:c.*3746_*3750delinsCCTTA	ENSP00000509254.1:n.*3746_*3750delinsCCTTA
ENST00000693560.1:c.*2423_*2427delinsCCTTA	ENSP00000509861.1:n.*2423_*2427delinsCCTTA
ENST00000371953.8:c.*2423_*2427delinsCCTTA MANE Select	ENSP00000361021.3:n.*2423_*2427delinsCCTTA
ENST00000371953.7:c.*2423_*2427delinsCCTTA	ENSP00000361021.3:n.*2423_*2427delinsCCTTA
NM_000314.5:c.*2423_*2427delinsCCTTA	NP_000305.3:n.*2423_*2427delinsCCTTA
NM_000314.6:c.*2423_*2427delinsCCTTA	NP_000305.3:n.*2423_*2427delinsCCTTA
NM_001304717.2:c.*2423_*2427delinsCCTTA	NP_001291646.2:n.*2423_*2427delinsCCTTA
NM_001304718.1:c.*2423_*2427delinsCCTTA	NP_001291647.1:n.*2423_*2427delinsCCTTA
XM_006717926.2:c.*2423_*2427delinsCCTTA	XP_006717989.1:n.*2423_*2427delinsCCTTA
XM_011539982.1:c.*2423_*2427delinsCCTTA	XP_011538284.1:n.*2423_*2427delinsCCTTA
XR_945791.1:n.4205_4209delinsCCTTA
NM_000314.7:c.*2423_*2427delinsCCTTA	NP_000305.3:n.*2423_*2427delinsCCTTA
NM_001304717.5:c.*2423_*2427delinsCCTTA	NP_001291646.4:n.*2423_*2427delinsCCTTA
NM_001304718.2:c.*2423_*2427delinsCCTTA	NP_001291647.1:n.*2423_*2427delinsCCTTA
NM_000314.8:c.*2423_*2427delinsCCTTA MANE Select	NP_000305.3:n.*2423_*2427delinsCCTTA