Canonical Allele Identifier: CA1926188572
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957954C= , CM000672.2:g.87957954C= GRCh38
NC_000010.10:g.89717711C= , CM000672.1:g.89717711C= GRCh37
NC_000010.9:g.89707691C= NCBI36
NG_007466.2:g.99516C= , LRG_311:g.99516C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.736C= ENSP00000514759.2:p.Pro246=
ENST00000710265.1:c.736C= ENSP00000518161.1:p.Pro246=
ENST00000472832.3:c.736C= ENSP00000483066.2:p.Pro246=
ENST00000688158.2:n.1471C=
ENST00000688922.2:c.*566C= ENSP00000508742.2:n.*566C=
ENST00000700021.1:c.691C= ENSP00000514757.1:p.Pro231=
ENST00000700022.1:c.*75C= ENSP00000514758.1:n.*75C=
ENST00000700023.1:n.1894C=
ENST00000700024.1:n.2128C=
ENST00000700025.1:n.1505C=
ENST00000700026.1:n.373C=
ENST00000700029.1:c.570C=
ENST00000706954.1:c.736C= ENSP00000516674.1:p.Pro246=
ENST00000706955.1:c.*771C= ENSP00000516675.1:n.*771C=
ENST00000686459.1:c.*322C= ENSP00000508909.1:n.*322C=
ENST00000688158.1:c.*847C= ENSP00000509254.1:n.*847C=
ENST00000688308.1:c.736C= ENSP00000508752.1:p.Pro246=
ENST00000688922.1:c.657C=
ENST00000693560.1:c.1255C= ENSP00000509861.1:p.Pro419=
ENST00000371953.8:c.736C= MANE Select ENSP00000361021.3:p.Pro246=
ENST00000371953.7:c.736C= ENSP00000361021.3:p.Pro246=
ENST00000472832.2:c.163C= ENSP00000483066.1:p.Pro55=
NM_000314.5:c.736C= NP_000305.3:p.Pro246=
NM_000314.6:c.736C= NP_000305.3:p.Pro246=
NM_001304717.2:c.1255C= NP_001291646.2:p.Pro419=
NM_001304718.1:c.145C= NP_001291647.1:p.Pro49=
XM_006717926.2:c.691C= XP_006717989.1:p.Pro231=
XM_011539981.1:c.736C= XP_011538283.1:p.Pro246=
XM_011539982.1:c.640C= XP_011538284.1:p.Pro214=
XR_945791.1:n.1306C=
NM_000314.7:c.736C= NP_000305.3:p.Pro246=
NM_001304717.5:c.1255C= NP_001291646.4:p.Pro419=
NM_001304718.2:c.145C= NP_001291647.1:p.Pro49=
NM_000314.8:c.736C= MANE Select NP_000305.3:p.Pro246=