Canonical Allele Identifier: CA1926177600

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967984_87967985delinsAT , CM000672.2:g.87967984_87967985delinsAT	GRCh38
NC_000010.10:g.89727741_89727742delinsAT , CM000672.1:g.89727741_89727742delinsAT	GRCh37
NC_000010.9:g.89717721_89717722delinsAT	NCBI36
NG_007466.2:g.109546_109547delinsAT , LRG_311:g.109546_109547delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2753_*2754delinsAT	ENSP00000518161.1:n.*2753_*2754delinsAT
ENST00000688158.2:n.4459_4460delinsAT
ENST00000706954.1:c.*2512_*2513delinsAT	ENSP00000516674.1:n.*2512_*2513delinsAT
ENST00000706955.1:c.*3759_*3760delinsAT	ENSP00000516675.1:n.*3759_*3760delinsAT
ENST00000688158.1:c.*3835_*3836delinsAT	ENSP00000509254.1:n.*3835_*3836delinsAT
ENST00000693560.1:c.*2512_*2513delinsAT	ENSP00000509861.1:n.*2512_*2513delinsAT
ENST00000371953.8:c.*2512_*2513delinsAT MANE Select	ENSP00000361021.3:n.*2512_*2513delinsAT
ENST00000371953.7:c.*2512_*2513delinsAT	ENSP00000361021.3:n.*2512_*2513delinsAT
NM_000314.5:c.*2512_*2513delinsAT	NP_000305.3:n.*2512_*2513delinsAT
NM_000314.6:c.*2512_*2513delinsAT	NP_000305.3:n.*2512_*2513delinsAT
NM_001304717.2:c.*2512_*2513delinsAT	NP_001291646.2:n.*2512_*2513delinsAT
NM_001304718.1:c.*2512_*2513delinsAT	NP_001291647.1:n.*2512_*2513delinsAT
XM_006717926.2:c.*2512_*2513delinsAT	XP_006717989.1:n.*2512_*2513delinsAT
XM_011539982.1:c.*2512_*2513delinsAT	XP_011538284.1:n.*2512_*2513delinsAT
XR_945791.1:n.4294_4295delinsAT
NM_000314.7:c.*2512_*2513delinsAT	NP_000305.3:n.*2512_*2513delinsAT
NM_001304717.5:c.*2512_*2513delinsAT	NP_001291646.4:n.*2512_*2513delinsAT
NM_001304718.2:c.*2512_*2513delinsAT	NP_001291647.1:n.*2512_*2513delinsAT
NM_000314.8:c.*2512_*2513delinsAT MANE Select	NP_000305.3:n.*2512_*2513delinsAT