Canonical Allele Identifier: CA891839436

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957882_87957884delinsTTT , CM000672.2:g.87957882_87957884delinsTTT	GRCh38
NC_000010.10:g.89717639_89717641delinsTTT , CM000672.1:g.89717639_89717641delinsTTT	GRCh37
NC_000010.9:g.89707619_89707621delinsTTT	NCBI36
NG_007466.2:g.99444_99446delinsTTT , LRG_311:g.99444_99446delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.664_666delinsTTT	ENSP00000514759.2:p.Val222Phe
ENST00000710265.1:c.664_666delinsTTT	ENSP00000518161.1:p.Val222Phe
ENST00000472832.3:c.664_666delinsTTT	ENSP00000483066.2:p.Val222Phe
ENST00000688158.2:n.1399_1401delinsTTT
ENST00000688922.2:c.*494_*496delinsTTT	ENSP00000508742.2:n.*494_*496delinsTTT
ENST00000700021.1:c.619_621delinsTTT	ENSP00000514757.1:p.Val207Phe
ENST00000700022.1:c.*3_*5delinsTTT	ENSP00000514758.1:n.*3_*5delinsTTT
ENST00000700023.1:n.1822_1824delinsTTT
ENST00000700024.1:n.2056_2058delinsTTT
ENST00000700025.1:n.1433_1435delinsTTT
ENST00000700026.1:n.301_303delinsTTT
ENST00000700029.1:c.498_500delinsTTT
ENST00000706954.1:c.664_666delinsTTT	ENSP00000516674.1:p.Val222Phe
ENST00000706955.1:c.*699_*701delinsTTT	ENSP00000516675.1:n.*699_*701delinsTTT
ENST00000686459.1:c.*250_*252delinsTTT	ENSP00000508909.1:n.*250_*252delinsTTT
ENST00000688158.1:c.*775_*777delinsTTT	ENSP00000509254.1:n.*775_*777delinsTTT
ENST00000688308.1:c.664_666delinsTTT	ENSP00000508752.1:p.Val222Phe
ENST00000688922.1:c.585_587delinsTTT
ENST00000693560.1:c.1183_1185delinsTTT	ENSP00000509861.1:p.Val395Phe
ENST00000371953.8:c.664_666delinsTTT MANE Select	ENSP00000361021.3:p.Val222Phe
ENST00000371953.7:c.664_666delinsTTT	ENSP00000361021.3:p.Val222Phe
ENST00000472832.2:c.91_93delinsTTT	ENSP00000483066.1:p.Val31Phe
NM_000314.5:c.664_666delinsTTT	NP_000305.3:p.Val222Phe
NM_000314.6:c.664_666delinsTTT	NP_000305.3:p.Val222Phe
NM_001304717.2:c.1183_1185delinsTTT	NP_001291646.2:p.Val395Phe
NM_001304718.1:c.73_75delinsTTT	NP_001291647.1:p.Val25Phe
XM_006717926.2:c.619_621delinsTTT	XP_006717989.1:p.Val207Phe
XM_011539981.1:c.664_666delinsTTT	XP_011538283.1:p.Val222Phe
XM_011539982.1:c.568_570delinsTTT	XP_011538284.1:p.Val190Phe
XR_945791.1:n.1234_1236delinsTTT
NM_000314.7:c.664_666delinsTTT	NP_000305.3:p.Val222Phe
NM_001304717.5:c.1183_1185delinsTTT	NP_001291646.4:p.Val395Phe
NM_001304718.2:c.73_75delinsTTT	NP_001291647.1:p.Val25Phe
NM_000314.8:c.664_666delinsTTT MANE Select	NP_000305.3:p.Val222Phe