Canonical Allele Identifier: CA1926182711
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952157T= , CM000672.2:g.87952157T= GRCh38
NC_000010.10:g.89711914T= , CM000672.1:g.89711914T= GRCh37
NC_000010.9:g.89701894T= NCBI36
NG_007466.2:g.93719T= , LRG_311:g.93719T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.532T= ENSP00000514759.2:p.Tyr178=
ENST00000710265.1:c.532T= ENSP00000518161.1:p.Tyr178=
ENST00000472832.3:c.532T= ENSP00000483066.2:p.Tyr178=
ENST00000688158.2:n.1267T=
ENST00000688922.2:c.*362T= ENSP00000508742.2:n.*362T=
ENST00000700021.1:c.487T= ENSP00000514757.1:p.Tyr163=
ENST00000700022.1:c.493-5696T= ENSP00000514758.1:n.493-5696T=
ENST00000700023.1:n.1690T=
ENST00000700024.1:n.1924T=
ENST00000700025.1:n.1301T=
ENST00000700029.1:c.366T=
ENST00000706954.1:c.532T= ENSP00000516674.1:p.Tyr178=
ENST00000706955.1:c.*567T= ENSP00000516675.1:n.*567T=
ENST00000686459.1:c.*118T= ENSP00000508909.1:n.*118T=
ENST00000688158.1:c.*643T= ENSP00000509254.1:n.*643T=
ENST00000688308.1:c.532T= ENSP00000508752.1:p.Tyr178=
ENST00000688922.1:c.453T=
ENST00000693560.1:c.1051T= ENSP00000509861.1:p.Tyr351=
ENST00000371953.8:c.532T= MANE Select ENSP00000361021.3:p.Tyr178=
ENST00000371953.7:c.532T= ENSP00000361021.3:p.Tyr178=
NM_000314.5:c.532T= NP_000305.3:p.Tyr178=
NM_000314.6:c.532T= NP_000305.3:p.Tyr178=
NM_001304717.2:c.1051T= NP_001291646.2:p.Tyr351=
NM_001304718.1:c.-60T= NP_001291647.1:n.-60T=
XM_006717926.2:c.487T= XP_006717989.1:p.Tyr163=
XM_011539981.1:c.532T= XP_011538283.1:p.Tyr178=
XM_011539982.1:c.436T= XP_011538284.1:p.Tyr146=
XR_945789.1:n.1403T=
XR_945790.1:n.1520T=
XR_945791.1:n.1205-5696T=
NM_000314.7:c.532T= NP_000305.3:p.Tyr178=
NM_001304717.5:c.1051T= NP_001291646.4:p.Tyr351=
NM_001304718.2:c.-60T= NP_001291647.1:n.-60T=
NM_000314.8:c.532T= MANE Select NP_000305.3:p.Tyr178=