Canonical Allele Identifier: CA1926190093

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961064_87961065delinsTC , CM000672.2:g.87961064_87961065delinsTC	GRCh38
NC_000010.10:g.89720821_89720822delinsTC , CM000672.1:g.89720821_89720822delinsTC	GRCh37
NC_000010.9:g.89710801_89710802delinsTC	NCBI36
NG_007466.2:g.102626_102627delinsTC , LRG_311:g.102626_102627delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1065_1066delinsTC	ENSP00000514759.2:p.Asp355=
ENST00000710265.1:c.972_973delinsTC	ENSP00000518161.1:p.Asp324=
ENST00000472832.3:c.972_973delinsTC	ENSP00000483066.2:p.Asp324=
ENST00000688158.2:n.1707_1708delinsTC
ENST00000688922.2:c.*802_*803delinsTC	ENSP00000508742.2:n.*802_*803delinsTC
ENST00000700021.1:c.927_928delinsTC	ENSP00000514757.1:p.Asp309=
ENST00000700022.1:c.*311_*312delinsTC	ENSP00000514758.1:n.*311_*312delinsTC
ENST00000700023.1:n.2130_2131delinsTC
ENST00000700024.1:n.2364_2365delinsTC
ENST00000700025.1:n.1741_1742delinsTC
ENST00000700026.1:n.609_610delinsTC
ENST00000706954.1:c.972_973delinsTC	ENSP00000516674.1:p.Asp324=
ENST00000706955.1:c.*1007_*1008delinsTC	ENSP00000516675.1:n.*1007_*1008delinsTC
ENST00000686459.1:c.*558_*559delinsTC	ENSP00000508909.1:n.*558_*559delinsTC
ENST00000688158.1:c.*1083_*1084delinsTC	ENSP00000509254.1:n.*1083_*1084delinsTC
ENST00000688308.1:c.972_973delinsTC	ENSP00000508752.1:p.Asp324=
ENST00000688922.1:c.893_894delinsTC
ENST00000693560.1:c.1491_1492delinsTC	ENSP00000509861.1:p.Asp497=
ENST00000371953.8:c.972_973delinsTC MANE Select	ENSP00000361021.3:p.Asp324=
ENST00000371953.7:c.972_973delinsTC	ENSP00000361021.3:p.Asp324=
ENST00000472832.2:c.399_400delinsTC	ENSP00000483066.1:p.Asp133=
NM_000314.5:c.972_973delinsTC	NP_000305.3:p.Asp324=
NM_000314.6:c.972_973delinsTC	NP_000305.3:p.Asp324=
NM_001304717.2:c.1491_1492delinsTC	NP_001291646.2:p.Asp497=
NM_001304718.1:c.381_382delinsTC	NP_001291647.1:p.Asp127=
XM_006717926.2:c.927_928delinsTC	XP_006717989.1:p.Asp309=
XM_011539981.1:c.972_973delinsTC	XP_011538283.1:p.Asp324=
XM_011539982.1:c.876_877delinsTC	XP_011538284.1:p.Asp292=
XR_945791.1:n.1542_1543delinsTC
NM_000314.7:c.972_973delinsTC	NP_000305.3:p.Asp324=
NM_001304717.5:c.1491_1492delinsTC	NP_001291646.4:p.Asp497=
NM_001304718.2:c.381_382delinsTC	NP_001291647.1:p.Asp127=
NM_000314.8:c.972_973delinsTC MANE Select	NP_000305.3:p.Asp324=