Canonical Allele Identifier: CA891837466

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965353_87965355delinsTTG , CM000672.2:g.87965353_87965355delinsTTG	GRCh38
NC_000010.10:g.89725110_89725112delinsTTG , CM000672.1:g.89725110_89725112delinsTTG	GRCh37
NC_000010.9:g.89715090_89715092delinsTTG	NCBI36
NG_007466.2:g.106915_106917delinsTTG , LRG_311:g.106915_106917delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1186_1188delinsTTG	ENSP00000514759.2:p.Val396Leu
ENST00000710265.1:c.*122_*124delinsTTG	ENSP00000518161.1:n.*122_*124delinsTTG
ENST00000688158.2:n.1828_1830delinsTTG
ENST00000688922.2:c.*923_*925delinsTTG	ENSP00000508742.2:n.*923_*925delinsTTG
ENST00000700021.1:c.1048_1050delinsTTG	ENSP00000514757.1:p.Val350Leu
ENST00000700022.1:c.*432_*434delinsTTG	ENSP00000514758.1:n.*432_*434delinsTTG
ENST00000700023.1:n.2251_2253delinsTTG
ENST00000700024.1:n.2485_2487delinsTTG
ENST00000706954.1:c.1093_1095delinsTTG	ENSP00000516674.1:p.Val365Leu
ENST00000706955.1:c.*1128_*1130delinsTTG	ENSP00000516675.1:n.*1128_*1130delinsTTG
ENST00000686459.1:c.*679_*681delinsTTG	ENSP00000508909.1:n.*679_*681delinsTTG
ENST00000688158.1:c.*1204_*1206delinsTTG	ENSP00000509254.1:n.*1204_*1206delinsTTG
ENST00000688308.1:c.1093_1095delinsTTG	ENSP00000508752.1:p.Val365Leu
ENST00000688922.1:c.1014_1016delinsTTG
ENST00000693560.1:c.1612_1614delinsTTG	ENSP00000509861.1:p.Val538Leu
ENST00000371953.8:c.1093_1095delinsTTG MANE Select	ENSP00000361021.3:p.Val365Leu
ENST00000371953.7:c.1093_1095delinsTTG	ENSP00000361021.3:p.Val365Leu
NM_000314.5:c.1093_1095delinsTTG	NP_000305.3:p.Val365Leu
NM_000314.6:c.1093_1095delinsTTG	NP_000305.3:p.Val365Leu
NM_001304717.2:c.1612_1614delinsTTG	NP_001291646.2:p.Val538Leu
NM_001304718.1:c.502_504delinsTTG	NP_001291647.1:p.Val168Leu
XM_006717926.2:c.1048_1050delinsTTG	XP_006717989.1:p.Val350Leu
XM_011539982.1:c.997_999delinsTTG	XP_011538284.1:p.Val333Leu
XR_945791.1:n.1663_1665delinsTTG
NM_000314.7:c.1093_1095delinsTTG	NP_000305.3:p.Val365Leu
NM_001304717.5:c.1612_1614delinsTTG	NP_001291646.4:p.Val538Leu
NM_001304718.2:c.502_504delinsTTG	NP_001291647.1:p.Val168Leu
NM_000314.8:c.1093_1095delinsTTG MANE Select	NP_000305.3:p.Val365Leu