Canonical Allele Identifier: CA1926182675
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952155A= , CM000672.2:g.87952155A= GRCh38
NC_000010.10:g.89711912A= , CM000672.1:g.89711912A= GRCh37
NC_000010.9:g.89701892A= NCBI36
NG_007466.2:g.93717A= , LRG_311:g.93717A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.530A= ENSP00000514759.2:p.Tyr177=
ENST00000710265.1:c.530A= ENSP00000518161.1:p.Tyr177=
ENST00000472832.3:c.530A= ENSP00000483066.2:p.Tyr177=
ENST00000688158.2:n.1265A=
ENST00000688922.2:c.*360A= ENSP00000508742.2:n.*360A=
ENST00000700021.1:c.485A= ENSP00000514757.1:p.Tyr162=
ENST00000700022.1:c.493-5698A= ENSP00000514758.1:n.493-5698A=
ENST00000700023.1:n.1688A=
ENST00000700024.1:n.1922A=
ENST00000700025.1:n.1299A=
ENST00000700029.1:c.364A=
ENST00000706954.1:c.530A= ENSP00000516674.1:p.Tyr177=
ENST00000706955.1:c.*565A= ENSP00000516675.1:n.*565A=
ENST00000686459.1:c.*116A= ENSP00000508909.1:n.*116A=
ENST00000688158.1:c.*641A= ENSP00000509254.1:n.*641A=
ENST00000688308.1:c.530A= ENSP00000508752.1:p.Tyr177=
ENST00000688922.1:c.451A=
ENST00000693560.1:c.1049A= ENSP00000509861.1:p.Tyr350=
ENST00000371953.8:c.530A= MANE Select ENSP00000361021.3:p.Tyr177=
ENST00000371953.7:c.530A= ENSP00000361021.3:p.Tyr177=
NM_000314.5:c.530A= NP_000305.3:p.Tyr177=
NM_000314.6:c.530A= NP_000305.3:p.Tyr177=
NM_001304717.2:c.1049A= NP_001291646.2:p.Tyr350=
NM_001304718.1:c.-62A= NP_001291647.1:n.-62A=
XM_006717926.2:c.485A= XP_006717989.1:p.Tyr162=
XM_011539981.1:c.530A= XP_011538283.1:p.Tyr177=
XM_011539982.1:c.434A= XP_011538284.1:p.Tyr145=
XR_945789.1:n.1401A=
XR_945790.1:n.1518A=
XR_945791.1:n.1205-5698A=
NM_000314.7:c.530A= NP_000305.3:p.Tyr177=
NM_001304717.5:c.1049A= NP_001291646.4:p.Tyr350=
NM_001304718.2:c.-62A= NP_001291647.1:n.-62A=
NM_000314.8:c.530A= MANE Select NP_000305.3:p.Tyr177=