Canonical Allele Identifier: CA891838784
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952154_87952155delinsGG , CM000672.2:g.87952154_87952155delinsGG GRCh38
NC_000010.10:g.89711911_89711912delinsGG , CM000672.1:g.89711911_89711912delinsGG GRCh37
NC_000010.9:g.89701891_89701892delinsGG NCBI36
NG_007466.2:g.93716_93717delinsGG , LRG_311:g.93716_93717delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.529_530delinsGG ENSP00000514759.2:p.Tyr177Gly
ENST00000710265.1:c.529_530delinsGG ENSP00000518161.1:p.Tyr177Gly
ENST00000472832.3:c.529_530delinsGG ENSP00000483066.2:p.Tyr177Gly
ENST00000688158.2:n.1264_1265delinsGG
ENST00000688922.2:c.*359_*360delinsGG ENSP00000508742.2:n.*359_*360delinsGG
ENST00000700021.1:c.484_485delinsGG ENSP00000514757.1:p.Tyr162Gly
ENST00000700022.1:c.493-5699_493-5698delinsGG ENSP00000514758.1:n.493-5699_493-5698delinsGG
ENST00000700023.1:n.1687_1688delinsGG
ENST00000700024.1:n.1921_1922delinsGG
ENST00000700025.1:n.1298_1299delinsGG
ENST00000700029.1:c.363_364delinsGG
ENST00000706954.1:c.529_530delinsGG ENSP00000516674.1:p.Tyr177Gly
ENST00000706955.1:c.*564_*565delinsGG ENSP00000516675.1:n.*564_*565delinsGG
ENST00000686459.1:c.*115_*116delinsGG ENSP00000508909.1:n.*115_*116delinsGG
ENST00000688158.1:c.*640_*641delinsGG ENSP00000509254.1:n.*640_*641delinsGG
ENST00000688308.1:c.529_530delinsGG ENSP00000508752.1:p.Tyr177Gly
ENST00000688922.1:c.450_451delinsGG
ENST00000693560.1:c.1048_1049delinsGG ENSP00000509861.1:p.Tyr350Gly
ENST00000371953.8:c.529_530delinsGG MANE Select ENSP00000361021.3:p.Tyr177Gly
ENST00000371953.7:c.529_530delinsGG ENSP00000361021.3:p.Tyr177Gly
NM_000314.5:c.529_530delinsGG NP_000305.3:p.Tyr177Gly
NM_000314.6:c.529_530delinsGG NP_000305.3:p.Tyr177Gly
NM_001304717.2:c.1048_1049delinsGG NP_001291646.2:p.Tyr350Gly
NM_001304718.1:c.-63_-62delinsGG NP_001291647.1:n.-63_-62delinsGG
XM_006717926.2:c.484_485delinsGG XP_006717989.1:p.Tyr162Gly
XM_011539981.1:c.529_530delinsGG XP_011538283.1:p.Tyr177Gly
XM_011539982.1:c.433_434delinsGG XP_011538284.1:p.Tyr145Gly
XR_945789.1:n.1400_1401delinsGG
XR_945790.1:n.1517_1518delinsGG
XR_945791.1:n.1205-5699_1205-5698delinsGG
NM_000314.7:c.529_530delinsGG NP_000305.3:p.Tyr177Gly
NM_001304717.5:c.1048_1049delinsGG NP_001291646.4:p.Tyr350Gly
NM_001304718.2:c.-63_-62delinsGG NP_001291647.1:n.-63_-62delinsGG
NM_000314.8:c.529_530delinsGG MANE Select NP_000305.3:p.Tyr177Gly