Canonical Allele Identifier: CA377484309
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs864622341

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952146A>T , CM000672.2:g.87952146A>T GRCh38
NC_000010.10:g.89711903A>T , CM000672.1:g.89711903A>T GRCh37
NC_000010.9:g.89701883A>T NCBI36
NG_007466.2:g.93708A>T , LRG_311:g.93708A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.521A>T ENSP00000514759.2:p.Tyr174Phe
ENST00000710265.1:c.521A>T ENSP00000518161.1:p.Tyr174Phe
ENST00000472832.3:c.521A>T ENSP00000483066.2:p.Tyr174Phe
ENST00000688158.2:n.1256A>T
ENST00000688922.2:c.*351A>T ENSP00000508742.2:n.*351A>T
ENST00000700021.1:c.476A>T ENSP00000514757.1:p.Tyr159Phe
ENST00000700022.1:c.493-5707A>T ENSP00000514758.1:n.493-5707A>T
ENST00000700023.1:n.1679A>T
ENST00000700024.1:n.1913A>T
ENST00000700025.1:n.1290A>T
ENST00000700029.1:c.355A>T
ENST00000706954.1:c.521A>T ENSP00000516674.1:p.Tyr174Phe
ENST00000706955.1:c.*556A>T ENSP00000516675.1:n.*556A>T
ENST00000686459.1:c.*107A>T ENSP00000508909.1:n.*107A>T
ENST00000688158.1:c.*632A>T ENSP00000509254.1:n.*632A>T
ENST00000688308.1:c.521A>T ENSP00000508752.1:p.Tyr174Phe
ENST00000688922.1:c.442A>T
ENST00000693560.1:c.1040A>T ENSP00000509861.1:p.Tyr347Phe
ENST00000371953.8:c.521A>T MANE Select ENSP00000361021.3:p.Tyr174Phe
ENST00000371953.7:c.521A>T ENSP00000361021.3:p.Tyr174Phe
NM_000314.5:c.521A>T NP_000305.3:p.Tyr174Phe
NM_000314.6:c.521A>T NP_000305.3:p.Tyr174Phe
NM_001304717.2:c.1040A>T NP_001291646.2:p.Tyr347Phe
NM_001304718.1:c.-71A>T NP_001291647.1:n.-71A>T
XM_006717926.2:c.476A>T XP_006717989.1:p.Tyr159Phe
XM_011539981.1:c.521A>T XP_011538283.1:p.Tyr174Phe
XM_011539982.1:c.425A>T XP_011538284.1:p.Tyr142Phe
XR_945789.1:n.1392A>T
XR_945790.1:n.1509A>T
XR_945791.1:n.1205-5707A>T
NM_000314.7:c.521A>T NP_000305.3:p.Tyr174Phe
NM_001304717.5:c.1040A>T NP_001291646.4:p.Tyr347Phe
NM_001304718.2:c.-71A>T NP_001291647.1:n.-71A>T
NM_000314.8:c.521A>T MANE Select NP_000305.3:p.Tyr174Phe