Canonical Allele Identifier: CA930911357
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1860805172

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967693C>T , CM000672.2:g.87967693C>T GRCh38
NC_000010.10:g.89727450C>T , CM000672.1:g.89727450C>T GRCh37
NC_000010.9:g.89717430C>T NCBI36
NG_007466.2:g.109255C>T , LRG_311:g.109255C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000710265.1:c.*2462C>T ENSP00000518161.1:n.*2462C>T
ENST00000688158.2:n.4168C>T
ENST00000706954.1:c.*2221C>T ENSP00000516674.1:n.*2221C>T
ENST00000706955.1:c.*3468C>T ENSP00000516675.1:n.*3468C>T
ENST00000688158.1:c.*3544C>T ENSP00000509254.1:n.*3544C>T
ENST00000693560.1:c.*2221C>T ENSP00000509861.1:n.*2221C>T
ENST00000371953.8:c.*2221C>T MANE Select ENSP00000361021.3:n.*2221C>T
ENST00000371953.7:c.*2221C>T ENSP00000361021.3:n.*2221C>T
NM_000314.5:c.*2221C>T NP_000305.3:n.*2221C>T
NM_000314.6:c.*2221C>T NP_000305.3:n.*2221C>T
NM_001304717.2:c.*2221C>T NP_001291646.2:n.*2221C>T
NM_001304718.1:c.*2221C>T NP_001291647.1:n.*2221C>T
XM_006717926.2:c.*2221C>T XP_006717989.1:n.*2221C>T
XM_011539982.1:c.*2221C>T XP_011538284.1:n.*2221C>T
XR_945791.1:n.4003C>T
NM_000314.7:c.*2221C>T NP_000305.3:n.*2221C>T
NM_001304717.5:c.*2221C>T NP_001291646.4:n.*2221C>T
NM_001304718.2:c.*2221C>T NP_001291647.1:n.*2221C>T
NM_000314.8:c.*2221C>T MANE Select NP_000305.3:n.*2221C>T