Canonical Allele Identifier: CA891838717

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952139_87952141delinsTAT , CM000672.2:g.87952139_87952141delinsTAT	GRCh38
NC_000010.10:g.89711896_89711898delinsTAT , CM000672.1:g.89711896_89711898delinsTAT	GRCh37
NC_000010.9:g.89701876_89701878delinsTAT	NCBI36
NG_007466.2:g.93701_93703delinsTAT , LRG_311:g.93701_93703delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.514_516delinsTAT	ENSP00000514759.2:p.Arg172Tyr
ENST00000710265.1:c.514_516delinsTAT	ENSP00000518161.1:p.Arg172Tyr
ENST00000472832.3:c.514_516delinsTAT	ENSP00000483066.2:p.Arg172Tyr
ENST00000688158.2:n.1249_1251delinsTAT
ENST00000688922.2:c.*344_*346delinsTAT	ENSP00000508742.2:n.*344_*346delinsTAT
ENST00000700021.1:c.469_471delinsTAT	ENSP00000514757.1:p.Arg157Tyr
ENST00000700022.1:c.493-5714_493-5712delinsTAT	ENSP00000514758.1:n.493-5714_493-5712delinsTAT
ENST00000700023.1:n.1672_1674delinsTAT
ENST00000700024.1:n.1906_1908delinsTAT
ENST00000700025.1:n.1283_1285delinsTAT
ENST00000700029.1:c.348_350delinsTAT
ENST00000706954.1:c.514_516delinsTAT	ENSP00000516674.1:p.Arg172Tyr
ENST00000706955.1:c.*549_*551delinsTAT	ENSP00000516675.1:n.*549_*551delinsTAT
ENST00000686459.1:c.*100_*102delinsTAT	ENSP00000508909.1:n.*100_*102delinsTAT
ENST00000688158.1:c.*625_*627delinsTAT	ENSP00000509254.1:n.*625_*627delinsTAT
ENST00000688308.1:c.514_516delinsTAT	ENSP00000508752.1:p.Arg172Tyr
ENST00000688922.1:c.435_437delinsTAT
ENST00000693560.1:c.1033_1035delinsTAT	ENSP00000509861.1:p.Arg345Tyr
ENST00000371953.8:c.514_516delinsTAT MANE Select	ENSP00000361021.3:p.Arg172Tyr
ENST00000371953.7:c.514_516delinsTAT	ENSP00000361021.3:p.Arg172Tyr
NM_000314.5:c.514_516delinsTAT	NP_000305.3:p.Arg172Tyr
NM_000314.6:c.514_516delinsTAT	NP_000305.3:p.Arg172Tyr
NM_001304717.2:c.1033_1035delinsTAT	NP_001291646.2:p.Arg345Tyr
NM_001304718.1:c.-78_-76delinsTAT	NP_001291647.1:n.-78_-76delinsTAT
XM_006717926.2:c.469_471delinsTAT	XP_006717989.1:p.Arg157Tyr
XM_011539981.1:c.514_516delinsTAT	XP_011538283.1:p.Arg172Tyr
XM_011539982.1:c.418_420delinsTAT	XP_011538284.1:p.Arg140Tyr
XR_945789.1:n.1385_1387delinsTAT
XR_945790.1:n.1502_1504delinsTAT
XR_945791.1:n.1205-5714_1205-5712delinsTAT
NM_000314.7:c.514_516delinsTAT	NP_000305.3:p.Arg172Tyr
NM_001304717.5:c.1033_1035delinsTAT	NP_001291646.4:p.Arg345Tyr
NM_001304718.2:c.-78_-76delinsTAT	NP_001291647.1:n.-78_-76delinsTAT
NM_000314.8:c.514_516delinsTAT MANE Select	NP_000305.3:p.Arg172Tyr