Canonical Allele Identifier: CA891838674

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952131_87952132delinsAT , CM000672.2:g.87952131_87952132delinsAT	GRCh38
NC_000010.10:g.89711888_89711889delinsAT , CM000672.1:g.89711888_89711889delinsAT	GRCh37
NC_000010.9:g.89701868_89701869delinsAT	NCBI36
NG_007466.2:g.93693_93694delinsAT , LRG_311:g.93693_93694delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.506_507delinsAT	ENSP00000514759.2:p.Pro169His
ENST00000710265.1:c.506_507delinsAT	ENSP00000518161.1:p.Pro169His
ENST00000472832.3:c.506_507delinsAT	ENSP00000483066.2:p.Pro169His
ENST00000688158.2:n.1241_1242delinsAT
ENST00000688922.2:c.*336_*337delinsAT	ENSP00000508742.2:n.*336_*337delinsAT
ENST00000700021.1:c.461_462delinsAT	ENSP00000514757.1:p.Pro154His
ENST00000700022.1:c.493-5722_493-5721delinsAT	ENSP00000514758.1:n.493-5722_493-5721delinsAT
ENST00000700023.1:n.1664_1665delinsAT
ENST00000700024.1:n.1898_1899delinsAT
ENST00000700025.1:n.1275_1276delinsAT
ENST00000700029.1:c.340_341delinsAT
ENST00000706954.1:c.506_507delinsAT	ENSP00000516674.1:p.Pro169His
ENST00000706955.1:c.*541_*542delinsAT	ENSP00000516675.1:n.*541_*542delinsAT
ENST00000686459.1:c.*92_*93delinsAT	ENSP00000508909.1:n.*92_*93delinsAT
ENST00000688158.1:c.*617_*618delinsAT	ENSP00000509254.1:n.*617_*618delinsAT
ENST00000688308.1:c.506_507delinsAT	ENSP00000508752.1:p.Pro169His
ENST00000688922.1:c.427_428delinsAT
ENST00000693560.1:c.1025_1026delinsAT	ENSP00000509861.1:p.Pro342His
ENST00000371953.8:c.506_507delinsAT MANE Select	ENSP00000361021.3:p.Pro169His
ENST00000371953.7:c.506_507delinsAT	ENSP00000361021.3:p.Pro169His
NM_000314.5:c.506_507delinsAT	NP_000305.3:p.Pro169His
NM_000314.6:c.506_507delinsAT	NP_000305.3:p.Pro169His
NM_001304717.2:c.1025_1026delinsAT	NP_001291646.2:p.Pro342His
NM_001304718.1:c.-86_-85delinsAT	NP_001291647.1:n.-86_-85delinsAT
XM_006717926.2:c.461_462delinsAT	XP_006717989.1:p.Pro154His
XM_011539981.1:c.506_507delinsAT	XP_011538283.1:p.Pro169His
XM_011539982.1:c.410_411delinsAT	XP_011538284.1:p.Pro137His
XR_945789.1:n.1377_1378delinsAT
XR_945790.1:n.1494_1495delinsAT
XR_945791.1:n.1205-5722_1205-5721delinsAT
NM_000314.7:c.506_507delinsAT	NP_000305.3:p.Pro169His
NM_001304717.5:c.1025_1026delinsAT	NP_001291646.4:p.Pro342His
NM_001304718.2:c.-86_-85delinsAT	NP_001291647.1:n.-86_-85delinsAT
NM_000314.8:c.506_507delinsAT MANE Select	NP_000305.3:p.Pro169His