Canonical Allele Identifier: CA1926188591
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957973A= , CM000672.2:g.87957973A= GRCh38
NC_000010.10:g.89717730A= , CM000672.1:g.89717730A= GRCh37
NC_000010.9:g.89707710A= NCBI36
NG_007466.2:g.99535A= , LRG_311:g.99535A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.755A= ENSP00000514759.2:p.Asp252=
ENST00000710265.1:c.755A= ENSP00000518161.1:p.Asp252=
ENST00000472832.3:c.755A= ENSP00000483066.2:p.Asp252=
ENST00000688158.2:n.1490A=
ENST00000688922.2:c.*585A= ENSP00000508742.2:n.*585A=
ENST00000700021.1:c.710A= ENSP00000514757.1:p.Asp237=
ENST00000700022.1:c.*94A= ENSP00000514758.1:n.*94A=
ENST00000700023.1:n.1913A=
ENST00000700024.1:n.2147A=
ENST00000700025.1:n.1524A=
ENST00000700026.1:n.392A=
ENST00000700029.1:c.589A=
ENST00000706954.1:c.755A= ENSP00000516674.1:p.Asp252=
ENST00000706955.1:c.*790A= ENSP00000516675.1:n.*790A=
ENST00000686459.1:c.*341A= ENSP00000508909.1:n.*341A=
ENST00000688158.1:c.*866A= ENSP00000509254.1:n.*866A=
ENST00000688308.1:c.755A= ENSP00000508752.1:p.Asp252=
ENST00000688922.1:c.676A=
ENST00000693560.1:c.1274A= ENSP00000509861.1:p.Asp425=
ENST00000371953.8:c.755A= MANE Select ENSP00000361021.3:p.Asp252=
ENST00000371953.7:c.755A= ENSP00000361021.3:p.Asp252=
ENST00000472832.2:c.182A= ENSP00000483066.1:p.Asp61=
NM_000314.5:c.755A= NP_000305.3:p.Asp252=
NM_000314.6:c.755A= NP_000305.3:p.Asp252=
NM_001304717.2:c.1274A= NP_001291646.2:p.Asp425=
NM_001304718.1:c.164A= NP_001291647.1:p.Asp55=
XM_006717926.2:c.710A= XP_006717989.1:p.Asp237=
XM_011539981.1:c.755A= XP_011538283.1:p.Asp252=
XM_011539982.1:c.659A= XP_011538284.1:p.Asp220=
XR_945791.1:n.1325A=
NM_000314.7:c.755A= NP_000305.3:p.Asp252=
NM_001304717.5:c.1274A= NP_001291646.4:p.Asp425=
NM_001304718.2:c.164A= NP_001291647.1:p.Asp55=
NM_000314.8:c.755A= MANE Select NP_000305.3:p.Asp252=