Canonical Allele Identifier: CA891837464

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965353_87965355delinsTAT , CM000672.2:g.87965353_87965355delinsTAT	GRCh38
NC_000010.10:g.89725110_89725112delinsTAT , CM000672.1:g.89725110_89725112delinsTAT	GRCh37
NC_000010.9:g.89715090_89715092delinsTAT	NCBI36
NG_007466.2:g.106915_106917delinsTAT , LRG_311:g.106915_106917delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1186_1188delinsTAT	ENSP00000514759.2:p.Val396Tyr
ENST00000710265.1:c.*122_*124delinsTAT	ENSP00000518161.1:n.*122_*124delinsTAT
ENST00000688158.2:n.1828_1830delinsTAT
ENST00000688922.2:c.*923_*925delinsTAT	ENSP00000508742.2:n.*923_*925delinsTAT
ENST00000700021.1:c.1048_1050delinsTAT	ENSP00000514757.1:p.Val350Tyr
ENST00000700022.1:c.*432_*434delinsTAT	ENSP00000514758.1:n.*432_*434delinsTAT
ENST00000700023.1:n.2251_2253delinsTAT
ENST00000700024.1:n.2485_2487delinsTAT
ENST00000706954.1:c.1093_1095delinsTAT	ENSP00000516674.1:p.Val365Tyr
ENST00000706955.1:c.*1128_*1130delinsTAT	ENSP00000516675.1:n.*1128_*1130delinsTAT
ENST00000686459.1:c.*679_*681delinsTAT	ENSP00000508909.1:n.*679_*681delinsTAT
ENST00000688158.1:c.*1204_*1206delinsTAT	ENSP00000509254.1:n.*1204_*1206delinsTAT
ENST00000688308.1:c.1093_1095delinsTAT	ENSP00000508752.1:p.Val365Tyr
ENST00000688922.1:c.1014_1016delinsTAT
ENST00000693560.1:c.1612_1614delinsTAT	ENSP00000509861.1:p.Val538Tyr
ENST00000371953.8:c.1093_1095delinsTAT MANE Select	ENSP00000361021.3:p.Val365Tyr
ENST00000371953.7:c.1093_1095delinsTAT	ENSP00000361021.3:p.Val365Tyr
NM_000314.5:c.1093_1095delinsTAT	NP_000305.3:p.Val365Tyr
NM_000314.6:c.1093_1095delinsTAT	NP_000305.3:p.Val365Tyr
NM_001304717.2:c.1612_1614delinsTAT	NP_001291646.2:p.Val538Tyr
NM_001304718.1:c.502_504delinsTAT	NP_001291647.1:p.Val168Tyr
XM_006717926.2:c.1048_1050delinsTAT	XP_006717989.1:p.Val350Tyr
XM_011539982.1:c.997_999delinsTAT	XP_011538284.1:p.Val333Tyr
XR_945791.1:n.1663_1665delinsTAT
NM_000314.7:c.1093_1095delinsTAT	NP_000305.3:p.Val365Tyr
NM_001304717.5:c.1612_1614delinsTAT	NP_001291646.4:p.Val538Tyr
NM_001304718.2:c.502_504delinsTAT	NP_001291647.1:p.Val168Tyr
NM_000314.8:c.1093_1095delinsTAT MANE Select	NP_000305.3:p.Val365Tyr