Canonical Allele Identifier: CA1926173968

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965389_87965393delinsTATAG , CM000672.2:g.87965389_87965393delinsTATAG	GRCh38
NC_000010.10:g.89725146_89725150delinsTATAG , CM000672.1:g.89725146_89725150delinsTATAG	GRCh37
NC_000010.9:g.89715126_89715130delinsTATAG	NCBI36
NG_007466.2:g.106951_106955delinsTATAG , LRG_311:g.106951_106955delinsTATAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1222_1226delinsTATAG	ENSP00000514759.2:p.Tyr408=
ENST00000710265.1:c.*158_*162delinsTATAG	ENSP00000518161.1:n.*158_*162delinsTATAG
ENST00000688158.2:n.1864_1868delinsTATAG
ENST00000688922.2:c.*959_*963delinsTATAG	ENSP00000508742.2:n.*959_*963delinsTATAG
ENST00000700021.1:c.1084_1088delinsTATAG	ENSP00000514757.1:p.Tyr362=
ENST00000700022.1:c.*468_*472delinsTATAG	ENSP00000514758.1:n.*468_*472delinsTATAG
ENST00000700023.1:n.2287_2291delinsTATAG
ENST00000700024.1:n.2521_2525delinsTATAG
ENST00000706954.1:c.1129_1133delinsTATAG	ENSP00000516674.1:p.Tyr377=
ENST00000706955.1:c.*1164_*1168delinsTATAG	ENSP00000516675.1:n.*1164_*1168delinsTATAG
ENST00000686459.1:c.*715_*719delinsTATAG	ENSP00000508909.1:n.*715_*719delinsTATAG
ENST00000688158.1:c.*1240_*1244delinsTATAG	ENSP00000509254.1:n.*1240_*1244delinsTATAG
ENST00000688308.1:c.1129_1133delinsTATAG	ENSP00000508752.1:p.Tyr377=
ENST00000688922.1:c.1050_1054delinsTATAG
ENST00000693560.1:c.1648_1652delinsTATAG	ENSP00000509861.1:p.Tyr550=
ENST00000371953.8:c.1129_1133delinsTATAG MANE Select	ENSP00000361021.3:p.Tyr377=
ENST00000371953.7:c.1129_1133delinsTATAG	ENSP00000361021.3:p.Tyr377=
NM_000314.5:c.1129_1133delinsTATAG	NP_000305.3:p.Tyr377=
NM_000314.6:c.1129_1133delinsTATAG	NP_000305.3:p.Tyr377=
NM_001304717.2:c.1648_1652delinsTATAG	NP_001291646.2:p.Tyr550=
NM_001304718.1:c.538_542delinsTATAG	NP_001291647.1:p.Tyr180=
XM_006717926.2:c.1084_1088delinsTATAG	XP_006717989.1:p.Tyr362=
XM_011539982.1:c.1033_1037delinsTATAG	XP_011538284.1:p.Tyr345=
XR_945791.1:n.1699_1703delinsTATAG
NM_000314.7:c.1129_1133delinsTATAG	NP_000305.3:p.Tyr377=
NM_001304717.5:c.1648_1652delinsTATAG	NP_001291646.4:p.Tyr550=
NM_001304718.2:c.538_542delinsTATAG	NP_001291647.1:p.Tyr180=
NM_000314.8:c.1129_1133delinsTATAG MANE Select	NP_000305.3:p.Tyr377=