Canonical Allele Identifier: CA891836786

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961071_87961073delinsTCT , CM000672.2:g.87961071_87961073delinsTCT	GRCh38
NC_000010.10:g.89720828_89720830delinsTCT , CM000672.1:g.89720828_89720830delinsTCT	GRCh37
NC_000010.9:g.89710808_89710810delinsTCT	NCBI36
NG_007466.2:g.102633_102635delinsTCT , LRG_311:g.102633_102635delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1072_1074delinsTCT	ENSP00000514759.2:p.Lys358Ser
ENST00000710265.1:c.979_981delinsTCT	ENSP00000518161.1:p.Lys327Ser
ENST00000472832.3:c.979_981delinsTCT	ENSP00000483066.2:p.Lys327Ser
ENST00000688158.2:n.1714_1716delinsTCT
ENST00000688922.2:c.*809_*811delinsTCT	ENSP00000508742.2:n.*809_*811delinsTCT
ENST00000700021.1:c.934_936delinsTCT	ENSP00000514757.1:p.Lys312Ser
ENST00000700022.1:c.*318_*320delinsTCT	ENSP00000514758.1:n.*318_*320delinsTCT
ENST00000700023.1:n.2137_2139delinsTCT
ENST00000700024.1:n.2371_2373delinsTCT
ENST00000700025.1:n.1748_1750delinsTCT
ENST00000700026.1:n.616_618delinsTCT
ENST00000706954.1:c.979_981delinsTCT	ENSP00000516674.1:p.Lys327Ser
ENST00000706955.1:c.*1014_*1016delinsTCT	ENSP00000516675.1:n.*1014_*1016delinsTCT
ENST00000686459.1:c.*565_*567delinsTCT	ENSP00000508909.1:n.*565_*567delinsTCT
ENST00000688158.1:c.*1090_*1092delinsTCT	ENSP00000509254.1:n.*1090_*1092delinsTCT
ENST00000688308.1:c.979_981delinsTCT	ENSP00000508752.1:p.Lys327Ser
ENST00000688922.1:c.900_902delinsTCT
ENST00000693560.1:c.1498_1500delinsTCT	ENSP00000509861.1:p.Lys500Ser
ENST00000371953.8:c.979_981delinsTCT MANE Select	ENSP00000361021.3:p.Lys327Ser
ENST00000371953.7:c.979_981delinsTCT	ENSP00000361021.3:p.Lys327Ser
ENST00000472832.2:c.406_408delinsTCT	ENSP00000483066.1:p.Lys136Ser
NM_000314.5:c.979_981delinsTCT	NP_000305.3:p.Lys327Ser
NM_000314.6:c.979_981delinsTCT	NP_000305.3:p.Lys327Ser
NM_001304717.2:c.1498_1500delinsTCT	NP_001291646.2:p.Lys500Ser
NM_001304718.1:c.388_390delinsTCT	NP_001291647.1:p.Lys130Ser
XM_006717926.2:c.934_936delinsTCT	XP_006717989.1:p.Lys312Ser
XM_011539981.1:c.979_981delinsTCT	XP_011538283.1:p.Lys327Ser
XM_011539982.1:c.883_885delinsTCT	XP_011538284.1:p.Lys295Ser
XR_945791.1:n.1549_1551delinsTCT
NM_000314.7:c.979_981delinsTCT	NP_000305.3:p.Lys327Ser
NM_001304717.5:c.1498_1500delinsTCT	NP_001291646.4:p.Lys500Ser
NM_001304718.2:c.388_390delinsTCT	NP_001291647.1:p.Lys130Ser
NM_000314.8:c.979_981delinsTCT MANE Select	NP_000305.3:p.Lys327Ser