Canonical Allele Identifier: CA891841235

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961017_87961018delinsTT , CM000672.2:g.87961017_87961018delinsTT	GRCh38
NC_000010.10:g.89720774_89720775delinsTT , CM000672.1:g.89720774_89720775delinsTT	GRCh37
NC_000010.9:g.89710754_89710755delinsTT	NCBI36
NG_007466.2:g.102579_102580delinsTT , LRG_311:g.102579_102580delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1018_1019delinsTT	ENSP00000514759.2:p.Ala340Leu
ENST00000710265.1:c.925_926delinsTT	ENSP00000518161.1:p.Ala309Leu
ENST00000472832.3:c.925_926delinsTT	ENSP00000483066.2:p.Ala309Leu
ENST00000688158.2:n.1660_1661delinsTT
ENST00000688922.2:c.*755_*756delinsTT	ENSP00000508742.2:n.*755_*756delinsTT
ENST00000700021.1:c.880_881delinsTT	ENSP00000514757.1:p.Ala294Leu
ENST00000700022.1:c.*264_*265delinsTT	ENSP00000514758.1:n.*264_*265delinsTT
ENST00000700023.1:n.2083_2084delinsTT
ENST00000700024.1:n.2317_2318delinsTT
ENST00000700025.1:n.1694_1695delinsTT
ENST00000700026.1:n.562_563delinsTT
ENST00000706954.1:c.925_926delinsTT	ENSP00000516674.1:p.Ala309Leu
ENST00000706955.1:c.*960_*961delinsTT	ENSP00000516675.1:n.*960_*961delinsTT
ENST00000686459.1:c.*511_*512delinsTT	ENSP00000508909.1:n.*511_*512delinsTT
ENST00000688158.1:c.*1036_*1037delinsTT	ENSP00000509254.1:n.*1036_*1037delinsTT
ENST00000688308.1:c.925_926delinsTT	ENSP00000508752.1:p.Ala309Leu
ENST00000688922.1:c.846_847delinsTT
ENST00000693560.1:c.1444_1445delinsTT	ENSP00000509861.1:p.Ala482Leu
ENST00000371953.8:c.925_926delinsTT MANE Select	ENSP00000361021.3:p.Ala309Leu
ENST00000371953.7:c.925_926delinsTT	ENSP00000361021.3:p.Ala309Leu
ENST00000472832.2:c.352_353delinsTT	ENSP00000483066.1:p.Ala118Leu
NM_000314.5:c.925_926delinsTT	NP_000305.3:p.Ala309Leu
NM_000314.6:c.925_926delinsTT	NP_000305.3:p.Ala309Leu
NM_001304717.2:c.1444_1445delinsTT	NP_001291646.2:p.Ala482Leu
NM_001304718.1:c.334_335delinsTT	NP_001291647.1:p.Ala112Leu
XM_006717926.2:c.880_881delinsTT	XP_006717989.1:p.Ala294Leu
XM_011539981.1:c.925_926delinsTT	XP_011538283.1:p.Ala309Leu
XM_011539982.1:c.829_830delinsTT	XP_011538284.1:p.Ala277Leu
XR_945791.1:n.1495_1496delinsTT
NM_000314.7:c.925_926delinsTT	NP_000305.3:p.Ala309Leu
NM_001304717.5:c.1444_1445delinsTT	NP_001291646.4:p.Ala482Leu
NM_001304718.2:c.334_335delinsTT	NP_001291647.1:p.Ala112Leu
NM_000314.8:c.925_926delinsTT MANE Select	NP_000305.3:p.Ala309Leu