Canonical Allele Identifier: CA891839892
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957969_87957971delinsATG , CM000672.2:g.87957969_87957971delinsATG GRCh38
NC_000010.10:g.89717726_89717728delinsATG , CM000672.1:g.89717726_89717728delinsATG GRCh37
NC_000010.9:g.89707706_89707708delinsATG NCBI36
NG_007466.2:g.99531_99533delinsATG , LRG_311:g.99531_99533delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.751_753delinsATG ENSP00000514759.2:p.Gly251Met
ENST00000710265.1:c.751_753delinsATG ENSP00000518161.1:p.Gly251Met
ENST00000472832.3:c.751_753delinsATG ENSP00000483066.2:p.Gly251Met
ENST00000688158.2:n.1486_1488delinsATG
ENST00000688922.2:c.*581_*583delinsATG ENSP00000508742.2:n.*581_*583delinsATG
ENST00000700021.1:c.706_708delinsATG ENSP00000514757.1:p.Gly236Met
ENST00000700022.1:c.*90_*92delinsATG ENSP00000514758.1:n.*90_*92delinsATG
ENST00000700023.1:n.1909_1911delinsATG
ENST00000700024.1:n.2143_2145delinsATG
ENST00000700025.1:n.1520_1522delinsATG
ENST00000700026.1:n.388_390delinsATG
ENST00000700029.1:c.585_587delinsATG
ENST00000706954.1:c.751_753delinsATG ENSP00000516674.1:p.Gly251Met
ENST00000706955.1:c.*786_*788delinsATG ENSP00000516675.1:n.*786_*788delinsATG
ENST00000686459.1:c.*337_*339delinsATG ENSP00000508909.1:n.*337_*339delinsATG
ENST00000688158.1:c.*862_*864delinsATG ENSP00000509254.1:n.*862_*864delinsATG
ENST00000688308.1:c.751_753delinsATG ENSP00000508752.1:p.Gly251Met
ENST00000688922.1:c.672_674delinsATG
ENST00000693560.1:c.1270_1272delinsATG ENSP00000509861.1:p.Gly424Met
ENST00000371953.8:c.751_753delinsATG MANE Select ENSP00000361021.3:p.Gly251Met
ENST00000371953.7:c.751_753delinsATG ENSP00000361021.3:p.Gly251Met
ENST00000472832.2:c.178_180delinsATG ENSP00000483066.1:p.Gly60Met
NM_000314.5:c.751_753delinsATG NP_000305.3:p.Gly251Met
NM_000314.6:c.751_753delinsATG NP_000305.3:p.Gly251Met
NM_001304717.2:c.1270_1272delinsATG NP_001291646.2:p.Gly424Met
NM_001304718.1:c.160_162delinsATG NP_001291647.1:p.Gly54Met
XM_006717926.2:c.706_708delinsATG XP_006717989.1:p.Gly236Met
XM_011539981.1:c.751_753delinsATG XP_011538283.1:p.Gly251Met
XM_011539982.1:c.655_657delinsATG XP_011538284.1:p.Gly219Met
XR_945791.1:n.1321_1323delinsATG
NM_000314.7:c.751_753delinsATG NP_000305.3:p.Gly251Met
NM_001304717.5:c.1270_1272delinsATG NP_001291646.4:p.Gly424Met
NM_001304718.2:c.160_162delinsATG NP_001291647.1:p.Gly54Met
NM_000314.8:c.751_753delinsATG MANE Select NP_000305.3:p.Gly251Met