Canonical Allele Identifier: CA891837435

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965350_87965352delinsCAA , CM000672.2:g.87965350_87965352delinsCAA	GRCh38
NC_000010.10:g.89725107_89725109delinsCAA , CM000672.1:g.89725107_89725109delinsCAA	GRCh37
NC_000010.9:g.89715087_89715089delinsCAA	NCBI36
NG_007466.2:g.106912_106914delinsCAA , LRG_311:g.106912_106914delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1183_1185delinsCAA	ENSP00000514759.2:p.Ser395Gln
ENST00000710265.1:c.*119_*121delinsCAA	ENSP00000518161.1:n.*119_*121delinsCAA
ENST00000688158.2:n.1825_1827delinsCAA
ENST00000688922.2:c.*920_*922delinsCAA	ENSP00000508742.2:n.*920_*922delinsCAA
ENST00000700021.1:c.1045_1047delinsCAA	ENSP00000514757.1:p.Ser349Gln
ENST00000700022.1:c.*429_*431delinsCAA	ENSP00000514758.1:n.*429_*431delinsCAA
ENST00000700023.1:n.2248_2250delinsCAA
ENST00000700024.1:n.2482_2484delinsCAA
ENST00000706954.1:c.1090_1092delinsCAA	ENSP00000516674.1:p.Ser364Gln
ENST00000706955.1:c.*1125_*1127delinsCAA	ENSP00000516675.1:n.*1125_*1127delinsCAA
ENST00000686459.1:c.*676_*678delinsCAA	ENSP00000508909.1:n.*676_*678delinsCAA
ENST00000688158.1:c.*1201_*1203delinsCAA	ENSP00000509254.1:n.*1201_*1203delinsCAA
ENST00000688308.1:c.1090_1092delinsCAA	ENSP00000508752.1:p.Ser364Gln
ENST00000688922.1:c.1011_1013delinsCAA
ENST00000693560.1:c.1609_1611delinsCAA	ENSP00000509861.1:p.Ser537Gln
ENST00000371953.8:c.1090_1092delinsCAA MANE Select	ENSP00000361021.3:p.Ser364Gln
ENST00000371953.7:c.1090_1092delinsCAA	ENSP00000361021.3:p.Ser364Gln
NM_000314.5:c.1090_1092delinsCAA	NP_000305.3:p.Ser364Gln
NM_000314.6:c.1090_1092delinsCAA	NP_000305.3:p.Ser364Gln
NM_001304717.2:c.1609_1611delinsCAA	NP_001291646.2:p.Ser537Gln
NM_001304718.1:c.499_501delinsCAA	NP_001291647.1:p.Ser167Gln
XM_006717926.2:c.1045_1047delinsCAA	XP_006717989.1:p.Ser349Gln
XM_011539982.1:c.994_996delinsCAA	XP_011538284.1:p.Ser332Gln
XR_945791.1:n.1660_1662delinsCAA
NM_000314.7:c.1090_1092delinsCAA	NP_000305.3:p.Ser364Gln
NM_001304717.5:c.1609_1611delinsCAA	NP_001291646.4:p.Ser537Gln
NM_001304718.2:c.499_501delinsCAA	NP_001291647.1:p.Ser167Gln
NM_000314.8:c.1090_1092delinsCAA MANE Select	NP_000305.3:p.Ser364Gln