Canonical Allele Identifier: CA1926182624
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952153T= , CM000672.2:g.87952153T= GRCh38
NC_000010.10:g.89711910T= , CM000672.1:g.89711910T= GRCh37
NC_000010.9:g.89701890T= NCBI36
NG_007466.2:g.93715T= , LRG_311:g.93715T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.528T= ENSP00000514759.2:p.Tyr176=
ENST00000710265.1:c.528T= ENSP00000518161.1:p.Tyr176=
ENST00000472832.3:c.528T= ENSP00000483066.2:p.Tyr176=
ENST00000688158.2:n.1263T=
ENST00000688922.2:c.*358T= ENSP00000508742.2:n.*358T=
ENST00000700021.1:c.483T= ENSP00000514757.1:p.Tyr161=
ENST00000700022.1:c.493-5700T= ENSP00000514758.1:n.493-5700T=
ENST00000700023.1:n.1686T=
ENST00000700024.1:n.1920T=
ENST00000700025.1:n.1297T=
ENST00000700029.1:c.362T=
ENST00000706954.1:c.528T= ENSP00000516674.1:p.Tyr176=
ENST00000706955.1:c.*563T= ENSP00000516675.1:n.*563T=
ENST00000686459.1:c.*114T= ENSP00000508909.1:n.*114T=
ENST00000688158.1:c.*639T= ENSP00000509254.1:n.*639T=
ENST00000688308.1:c.528T= ENSP00000508752.1:p.Tyr176=
ENST00000688922.1:c.449T=
ENST00000693560.1:c.1047T= ENSP00000509861.1:p.Tyr349=
ENST00000371953.8:c.528T= MANE Select ENSP00000361021.3:p.Tyr176=
ENST00000371953.7:c.528T= ENSP00000361021.3:p.Tyr176=
NM_000314.5:c.528T= NP_000305.3:p.Tyr176=
NM_000314.6:c.528T= NP_000305.3:p.Tyr176=
NM_001304717.2:c.1047T= NP_001291646.2:p.Tyr349=
NM_001304718.1:c.-64T= NP_001291647.1:n.-64T=
XM_006717926.2:c.483T= XP_006717989.1:p.Tyr161=
XM_011539981.1:c.528T= XP_011538283.1:p.Tyr176=
XM_011539982.1:c.432T= XP_011538284.1:p.Tyr144=
XR_945789.1:n.1399T=
XR_945790.1:n.1516T=
XR_945791.1:n.1205-5700T=
NM_000314.7:c.528T= NP_000305.3:p.Tyr176=
NM_001304717.5:c.1047T= NP_001291646.4:p.Tyr349=
NM_001304718.2:c.-64T= NP_001291647.1:n.-64T=
NM_000314.8:c.528T= MANE Select NP_000305.3:p.Tyr176=