Canonical Allele Identifier: CA891838768

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952149_87952150delinsAT , CM000672.2:g.87952149_87952150delinsAT	GRCh38
NC_000010.10:g.89711906_89711907delinsAT , CM000672.1:g.89711906_89711907delinsAT	GRCh37
NC_000010.9:g.89701886_89701887delinsAT	NCBI36
NG_007466.2:g.93711_93712delinsAT , LRG_311:g.93711_93712delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.524_525delinsAT	ENSP00000514759.2:p.Val175Asp
ENST00000710265.1:c.524_525delinsAT	ENSP00000518161.1:p.Val175Asp
ENST00000472832.3:c.524_525delinsAT	ENSP00000483066.2:p.Val175Asp
ENST00000688158.2:n.1259_1260delinsAT
ENST00000688922.2:c.*354_*355delinsAT	ENSP00000508742.2:n.*354_*355delinsAT
ENST00000700021.1:c.479_480delinsAT	ENSP00000514757.1:p.Val160Asp
ENST00000700022.1:c.493-5704_493-5703delinsAT	ENSP00000514758.1:n.493-5704_493-5703delinsAT
ENST00000700023.1:n.1682_1683delinsAT
ENST00000700024.1:n.1916_1917delinsAT
ENST00000700025.1:n.1293_1294delinsAT
ENST00000700029.1:c.358_359delinsAT
ENST00000706954.1:c.524_525delinsAT	ENSP00000516674.1:p.Val175Asp
ENST00000706955.1:c.*559_*560delinsAT	ENSP00000516675.1:n.*559_*560delinsAT
ENST00000686459.1:c.*110_*111delinsAT	ENSP00000508909.1:n.*110_*111delinsAT
ENST00000688158.1:c.*635_*636delinsAT	ENSP00000509254.1:n.*635_*636delinsAT
ENST00000688308.1:c.524_525delinsAT	ENSP00000508752.1:p.Val175Asp
ENST00000688922.1:c.445_446delinsAT
ENST00000693560.1:c.1043_1044delinsAT	ENSP00000509861.1:p.Val348Asp
ENST00000371953.8:c.524_525delinsAT MANE Select	ENSP00000361021.3:p.Val175Asp
ENST00000371953.7:c.524_525delinsAT	ENSP00000361021.3:p.Val175Asp
NM_000314.5:c.524_525delinsAT	NP_000305.3:p.Val175Asp
NM_000314.6:c.524_525delinsAT	NP_000305.3:p.Val175Asp
NM_001304717.2:c.1043_1044delinsAT	NP_001291646.2:p.Val348Asp
NM_001304718.1:c.-68_-67delinsAT	NP_001291647.1:n.-68_-67delinsAT
XM_006717926.2:c.479_480delinsAT	XP_006717989.1:p.Val160Asp
XM_011539981.1:c.524_525delinsAT	XP_011538283.1:p.Val175Asp
XM_011539982.1:c.428_429delinsAT	XP_011538284.1:p.Val143Asp
XR_945789.1:n.1395_1396delinsAT
XR_945790.1:n.1512_1513delinsAT
XR_945791.1:n.1205-5704_1205-5703delinsAT
NM_000314.7:c.524_525delinsAT	NP_000305.3:p.Val175Asp
NM_001304717.5:c.1043_1044delinsAT	NP_001291646.4:p.Val348Asp
NM_001304718.2:c.-68_-67delinsAT	NP_001291647.1:n.-68_-67delinsAT
NM_000314.8:c.524_525delinsAT MANE Select	NP_000305.3:p.Val175Asp