Canonical Allele Identifier: CA1926186580
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87954224_87954225delinsTA , CM000672.2:g.87954224_87954225delinsTA GRCh38
NC_000010.10:g.89713981_89713982delinsTA , CM000672.1:g.89713981_89713982delinsTA GRCh37
NC_000010.9:g.89703961_89703962delinsTA NCBI36
NG_007466.2:g.95786_95787delinsTA , LRG_311:g.95786_95787delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.634+1965_634+1966delinsTA ENSP00000514759.2:n.634+1965_634+1966delinsTA
ENST00000710265.1:c.634+1965_634+1966delinsTA ENSP00000518161.1:n.634+1965_634+1966delinsTA
ENST00000472832.3:c.634+1965_634+1966delinsTA ENSP00000483066.2:n.634+1965_634+1966delinsTA
ENST00000688158.2:n.1369+1965_1369+1966delinsTA
ENST00000688922.2:c.*464+1965_*464+1966delinsTA ENSP00000508742.2:n.*464+1965_*464+1966delinsTA
ENST00000700021.1:c.589+1965_589+1966delinsTA ENSP00000514757.1:n.589+1965_589+1966delinsTA
ENST00000700022.1:c.493-3629_493-3628delinsTA ENSP00000514758.1:n.493-3629_493-3628delinsTA
ENST00000700023.1:n.1792+1965_1792+1966delinsTA
ENST00000700024.1:n.2026+1965_2026+1966delinsTA
ENST00000700025.1:n.1403+1965_1403+1966delinsTA
ENST00000700029.1:c.468+1965_468+1966delinsTA
ENST00000706954.1:c.634+1965_634+1966delinsTA ENSP00000516674.1:n.634+1965_634+1966delinsTA
ENST00000706955.1:c.*669+1965_*669+1966delinsTA ENSP00000516675.1:n.*669+1965_*669+1966delinsTA
ENST00000686459.1:c.*220+1965_*220+1966delinsTA ENSP00000508909.1:n.*220+1965_*220+1966delinsTA
ENST00000688158.1:c.*745+1965_*745+1966delinsTA ENSP00000509254.1:n.*745+1965_*745+1966delinsTA
ENST00000688308.1:c.634+1965_634+1966delinsTA ENSP00000508752.1:n.634+1965_634+1966delinsTA
ENST00000688922.1:c.555+1965_555+1966delinsTA
ENST00000693560.1:c.1153+1965_1153+1966delinsTA ENSP00000509861.1:n.1153+1965_1153+1966delinsTA
ENST00000371953.8:c.634+1965_634+1966delinsTA MANE Select ENSP00000361021.3:n.634+1965_634+1966delinsTA
ENST00000371953.7:c.634+1965_634+1966delinsTA ENSP00000361021.3:n.634+1965_634+1966delinsTA
ENST00000472832.2:c.61+1965_61+1966delinsTA ENSP00000483066.1:n.61+1965_61+1966delinsTA
NM_000314.5:c.634+1965_634+1966delinsTA NP_000305.3:n.634+1965_634+1966delinsTA
NM_000314.6:c.634+1965_634+1966delinsTA NP_000305.3:n.634+1965_634+1966delinsTA
NM_001304717.2:c.1153+1965_1153+1966delinsTA NP_001291646.2:n.1153+1965_1153+1966delinsTA
NM_001304718.1:c.43+1965_43+1966delinsTA NP_001291647.1:n.43+1965_43+1966delinsTA
XM_006717926.2:c.589+1965_589+1966delinsTA XP_006717989.1:n.589+1965_589+1966delinsTA
XM_011539981.1:c.634+1965_634+1966delinsTA XP_011538283.1:n.634+1965_634+1966delinsTA
XM_011539982.1:c.538+1965_538+1966delinsTA XP_011538284.1:n.538+1965_538+1966delinsTA
XR_945791.1:n.1205-3629_1205-3628delinsTA
NM_000314.7:c.634+1965_634+1966delinsTA NP_000305.3:n.634+1965_634+1966delinsTA
NM_001304717.5:c.1153+1965_1153+1966delinsTA NP_001291646.4:n.1153+1965_1153+1966delinsTA
NM_001304718.2:c.43+1965_43+1966delinsTA NP_001291647.1:n.43+1965_43+1966delinsTA
NM_000314.8:c.634+1965_634+1966delinsTA MANE Select NP_000305.3:n.634+1965_634+1966delinsTA