Canonical Allele Identifier: CA1926176692

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967420_87967422delinsCTT , CM000672.2:g.87967420_87967422delinsCTT	GRCh38
NC_000010.10:g.89727177_89727179delinsCTT , CM000672.1:g.89727177_89727179delinsCTT	GRCh37
NC_000010.9:g.89717157_89717159delinsCTT	NCBI36
NG_007466.2:g.108982_108984delinsCTT , LRG_311:g.108982_108984delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*2189_*2191delinsCTT	ENSP00000518161.1:n.*2189_*2191delinsCTT
ENST00000688158.2:n.3895_3897delinsCTT
ENST00000706954.1:c.*1948_*1950delinsCTT	ENSP00000516674.1:n.*1948_*1950delinsCTT
ENST00000706955.1:c.*3195_*3197delinsCTT	ENSP00000516675.1:n.*3195_*3197delinsCTT
ENST00000688158.1:c.*3271_*3273delinsCTT	ENSP00000509254.1:n.*3271_*3273delinsCTT
ENST00000693560.1:c.*1948_*1950delinsCTT	ENSP00000509861.1:n.*1948_*1950delinsCTT
ENST00000371953.8:c.*1948_*1950delinsCTT MANE Select	ENSP00000361021.3:n.*1948_*1950delinsCTT
ENST00000371953.7:c.*1948_*1950delinsCTT	ENSP00000361021.3:n.*1948_*1950delinsCTT
NM_000314.5:c.*1948_*1950delinsCTT	NP_000305.3:n.*1948_*1950delinsCTT
NM_000314.6:c.*1948_*1950delinsCTT	NP_000305.3:n.*1948_*1950delinsCTT
NM_001304717.2:c.*1948_*1950delinsCTT	NP_001291646.2:n.*1948_*1950delinsCTT
NM_001304718.1:c.*1948_*1950delinsCTT	NP_001291647.1:n.*1948_*1950delinsCTT
XM_006717926.2:c.*1948_*1950delinsCTT	XP_006717989.1:n.*1948_*1950delinsCTT
XM_011539982.1:c.*1948_*1950delinsCTT	XP_011538284.1:n.*1948_*1950delinsCTT
XR_945791.1:n.3730_3732delinsCTT
NM_000314.7:c.*1948_*1950delinsCTT	NP_000305.3:n.*1948_*1950delinsCTT
NM_001304717.5:c.*1948_*1950delinsCTT	NP_001291646.4:n.*1948_*1950delinsCTT
NM_001304718.2:c.*1948_*1950delinsCTT	NP_001291647.1:n.*1948_*1950delinsCTT
NM_000314.8:c.*1948_*1950delinsCTT MANE Select	NP_000305.3:n.*1948_*1950delinsCTT