Canonical Allele Identifier: CA891836491

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961042_87961043delinsGT , CM000672.2:g.87961042_87961043delinsGT	GRCh38
NC_000010.10:g.89720799_89720800delinsGT , CM000672.1:g.89720799_89720800delinsGT	GRCh37
NC_000010.9:g.89710779_89710780delinsGT	NCBI36
NG_007466.2:g.102604_102605delinsGT , LRG_311:g.102604_102605delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1043_1044delinsGT	ENSP00000514759.2:p.Val348Gly
ENST00000710265.1:c.950_951delinsGT	ENSP00000518161.1:p.Val317Gly
ENST00000472832.3:c.950_951delinsGT	ENSP00000483066.2:p.Val317Gly
ENST00000688158.2:n.1685_1686delinsGT
ENST00000688922.2:c.*780_*781delinsGT	ENSP00000508742.2:n.*780_*781delinsGT
ENST00000700021.1:c.905_906delinsGT	ENSP00000514757.1:p.Val302Gly
ENST00000700022.1:c.*289_*290delinsGT	ENSP00000514758.1:n.*289_*290delinsGT
ENST00000700023.1:n.2108_2109delinsGT
ENST00000700024.1:n.2342_2343delinsGT
ENST00000700025.1:n.1719_1720delinsGT
ENST00000700026.1:n.587_588delinsGT
ENST00000706954.1:c.950_951delinsGT	ENSP00000516674.1:p.Val317Gly
ENST00000706955.1:c.*985_*986delinsGT	ENSP00000516675.1:n.*985_*986delinsGT
ENST00000686459.1:c.*536_*537delinsGT	ENSP00000508909.1:n.*536_*537delinsGT
ENST00000688158.1:c.*1061_*1062delinsGT	ENSP00000509254.1:n.*1061_*1062delinsGT
ENST00000688308.1:c.950_951delinsGT	ENSP00000508752.1:p.Val317Gly
ENST00000688922.1:c.871_872delinsGT
ENST00000693560.1:c.1469_1470delinsGT	ENSP00000509861.1:p.Val490Gly
ENST00000371953.8:c.950_951delinsGT MANE Select	ENSP00000361021.3:p.Val317Gly
ENST00000371953.7:c.950_951delinsGT	ENSP00000361021.3:p.Val317Gly
ENST00000472832.2:c.377_378delinsGT	ENSP00000483066.1:p.Val126Gly
NM_000314.5:c.950_951delinsGT	NP_000305.3:p.Val317Gly
NM_000314.6:c.950_951delinsGT	NP_000305.3:p.Val317Gly
NM_001304717.2:c.1469_1470delinsGT	NP_001291646.2:p.Val490Gly
NM_001304718.1:c.359_360delinsGT	NP_001291647.1:p.Val120Gly
XM_006717926.2:c.905_906delinsGT	XP_006717989.1:p.Val302Gly
XM_011539981.1:c.950_951delinsGT	XP_011538283.1:p.Val317Gly
XM_011539982.1:c.854_855delinsGT	XP_011538284.1:p.Val285Gly
XR_945791.1:n.1520_1521delinsGT
NM_000314.7:c.950_951delinsGT	NP_000305.3:p.Val317Gly
NM_001304717.5:c.1469_1470delinsGT	NP_001291646.4:p.Val490Gly
NM_001304718.2:c.359_360delinsGT	NP_001291647.1:p.Val120Gly
NM_000314.8:c.950_951delinsGT MANE Select	NP_000305.3:p.Val317Gly