Canonical Allele Identifier: CA1926177038
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1644318974

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967621G>T , CM000672.2:g.87967621G>T GRCh38
NC_000010.10:g.89727378G>T , CM000672.1:g.89727378G>T GRCh37
NC_000010.9:g.89717358G>T NCBI36
NG_007466.2:g.109183G>T , LRG_311:g.109183G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000710265.1:c.*2390G>T ENSP00000518161.1:n.*2390G>T
ENST00000688158.2:n.4096G>T
ENST00000706954.1:c.*2149G>T ENSP00000516674.1:n.*2149G>T
ENST00000706955.1:c.*3396G>T ENSP00000516675.1:n.*3396G>T
ENST00000688158.1:c.*3472G>T ENSP00000509254.1:n.*3472G>T
ENST00000693560.1:c.*2149G>T ENSP00000509861.1:n.*2149G>T
ENST00000371953.8:c.*2149G>T MANE Select ENSP00000361021.3:n.*2149G>T
ENST00000371953.7:c.*2149G>T ENSP00000361021.3:n.*2149G>T
NM_000314.5:c.*2149G>T NP_000305.3:n.*2149G>T
NM_000314.6:c.*2149G>T NP_000305.3:n.*2149G>T
NM_001304717.2:c.*2149G>T NP_001291646.2:n.*2149G>T
NM_001304718.1:c.*2149G>T NP_001291647.1:n.*2149G>T
XM_006717926.2:c.*2149G>T XP_006717989.1:n.*2149G>T
XM_011539982.1:c.*2149G>T XP_011538284.1:n.*2149G>T
XR_945791.1:n.3931G>T
NM_000314.7:c.*2149G>T NP_000305.3:n.*2149G>T
NM_001304717.5:c.*2149G>T NP_001291646.4:n.*2149G>T
NM_001304718.2:c.*2149G>T NP_001291647.1:n.*2149G>T
NM_000314.8:c.*2149G>T MANE Select NP_000305.3:n.*2149G>T