Canonical Allele Identifier: CA470669975
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1554825245
MyVariant Identifiers: chr10:g.89717746C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957989C>T , CM000672.2:g.87957989C>T GRCh38
NC_000010.10:g.89717746C>T , CM000672.1:g.89717746C>T GRCh37
NC_000010.9:g.89707726C>T NCBI36
NG_007466.2:g.99551C>T , LRG_311:g.99551C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.771C>T ENSP00000514759.2:p.Phe257=
ENST00000710265.1:c.771C>T ENSP00000518161.1:p.Phe257=
ENST00000472832.3:c.771C>T ENSP00000483066.2:p.Phe257=
ENST00000688158.2:n.1506C>T
ENST00000688922.2:c.*601C>T ENSP00000508742.2:n.*601C>T
ENST00000700021.1:c.726C>T ENSP00000514757.1:p.Phe242=
ENST00000700022.1:c.*110C>T ENSP00000514758.1:n.*110C>T
ENST00000700023.1:n.1929C>T
ENST00000700024.1:n.2163C>T
ENST00000700025.1:n.1540C>T
ENST00000700026.1:n.408C>T
ENST00000700029.1:c.605C>T
ENST00000706954.1:c.771C>T ENSP00000516674.1:p.Phe257=
ENST00000706955.1:c.*806C>T ENSP00000516675.1:n.*806C>T
ENST00000686459.1:c.*357C>T ENSP00000508909.1:n.*357C>T
ENST00000688158.1:c.*882C>T ENSP00000509254.1:n.*882C>T
ENST00000688308.1:c.771C>T ENSP00000508752.1:p.Phe257=
ENST00000688922.1:c.692C>T
ENST00000693560.1:c.1290C>T ENSP00000509861.1:p.Phe430=
ENST00000371953.8:c.771C>T MANE Select ENSP00000361021.3:p.Phe257=
ENST00000371953.7:c.771C>T ENSP00000361021.3:p.Phe257=
ENST00000472832.2:c.198C>T ENSP00000483066.1:p.Phe66=
NM_000314.5:c.771C>T NP_000305.3:p.Phe257=
NM_000314.6:c.771C>T NP_000305.3:p.Phe257=
NM_001304717.2:c.1290C>T NP_001291646.2:p.Phe430=
NM_001304718.1:c.180C>T NP_001291647.1:p.Phe60=
XM_006717926.2:c.726C>T XP_006717989.1:p.Phe242=
XM_011539981.1:c.771C>T XP_011538283.1:p.Phe257=
XM_011539982.1:c.675C>T XP_011538284.1:p.Phe225=
XR_945791.1:n.1341C>T
NM_000314.7:c.771C>T NP_000305.3:p.Phe257=
NM_001304717.5:c.1290C>T NP_001291646.4:p.Phe430=
NM_001304718.2:c.180C>T NP_001291647.1:p.Phe60=
NM_000314.8:c.771C>T MANE Select NP_000305.3:p.Phe257=