Canonical Allele Identifier: CA377484965
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1860546467

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.736C>G ENSP00000514759.2:p.Pro246Ala
ENST00000710265.1:c.736C>G ENSP00000518161.1:p.Pro246Ala
ENST00000472832.3:c.736C>G ENSP00000483066.2:p.Pro246Ala
ENST00000688158.2:n.1471C>G
ENST00000688922.2:c.*566C>G ENSP00000508742.2:n.*566C>G
ENST00000700021.1:c.691C>G ENSP00000514757.1:p.Pro231Ala
ENST00000700022.1:c.*75C>G ENSP00000514758.1:n.*75C>G
ENST00000700023.1:n.1894C>G
ENST00000700024.1:n.2128C>G
ENST00000700025.1:n.1505C>G
ENST00000700026.1:n.373C>G
ENST00000700029.1:c.570C>G
ENST00000706954.1:c.736C>G ENSP00000516674.1:p.Pro246Ala
ENST00000706955.1:c.*771C>G ENSP00000516675.1:n.*771C>G
ENST00000686459.1:c.*322C>G ENSP00000508909.1:n.*322C>G
ENST00000688158.1:c.*847C>G ENSP00000509254.1:n.*847C>G
ENST00000688308.1:c.736C>G ENSP00000508752.1:p.Pro246Ala
ENST00000688922.1:c.657C>G
ENST00000693560.1:c.1255C>G ENSP00000509861.1:p.Pro419Ala
ENST00000371953.8:c.736C>G MANE Select ENSP00000361021.3:p.Pro246Ala
ENST00000371953.7:c.736C>G ENSP00000361021.3:p.Pro246Ala
ENST00000472832.2:c.163C>G ENSP00000483066.1:p.Pro55Ala
NM_000314.5:c.736C>G NP_000305.3:p.Pro246Ala
NM_000314.6:c.736C>G NP_000305.3:p.Pro246Ala
NM_001304717.2:c.1255C>G NP_001291646.2:p.Pro419Ala
NM_001304718.1:c.145C>G NP_001291647.1:p.Pro49Ala
XM_006717926.2:c.691C>G XP_006717989.1:p.Pro231Ala
XM_011539981.1:c.736C>G XP_011538283.1:p.Pro246Ala
XM_011539982.1:c.640C>G XP_011538284.1:p.Pro214Ala
XR_945791.1:n.1306C>G
NM_000314.7:c.736C>G NP_000305.3:p.Pro246Ala
NM_001304717.5:c.1255C>G NP_001291646.4:p.Pro419Ala
NM_001304718.2:c.145C>G NP_001291647.1:p.Pro49Ala
NM_000314.8:c.736C>G MANE Select NP_000305.3:p.Pro246Ala