Canonical Allele Identifier: CA1926189835
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960782_87960785delinsCTTT , CM000672.2:g.87960782_87960785delinsCTTT GRCh38
NC_000010.10:g.89720539_89720542delinsCTTT , CM000672.1:g.89720539_89720542delinsCTTT GRCh37
NC_000010.9:g.89710519_89710522delinsCTTT NCBI36
NG_007466.2:g.102344_102347delinsCTTT , LRG_311:g.102344_102347delinsCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.895-112_895-109delinsCTTT ENSP00000514759.2:n.895-112_895-109delins...
ENST00000710265.1:c.802-112_802-109delinsCTTT ENSP00000518161.1:n.802-112_802-109delins...
ENST00000472832.3:c.802-112_802-109delinsCTTT ENSP00000483066.2:n.802-112_802-109delins...
ENST00000688158.2:n.1537-112_1537-109delinsCTTT
ENST00000688922.2:c.*632-112_*632-109delinsCTTT ENSP00000508742.2:n.*632-112_*632-109deli...
ENST00000700021.1:c.757-112_757-109delinsCTTT ENSP00000514757.1:n.757-112_757-109delins...
ENST00000700022.1:c.*141-112_*141-109delinsCTTT ENSP00000514758.1:n.*141-112_*141-109deli...
ENST00000700023.1:n.1960-112_1960-109delinsCTTT
ENST00000700024.1:n.2194-112_2194-109delinsCTTT
ENST00000700025.1:n.1571-112_1571-109delinsCTTT
ENST00000700026.1:n.439-112_439-109delinsCTTT
ENST00000700029.1:c.729-112_729-109delinsCTTT
ENST00000706954.1:c.802-112_802-109delinsCTTT ENSP00000516674.1:n.802-112_802-109delins...
ENST00000706955.1:c.*837-112_*837-109delinsCTTT ENSP00000516675.1:n.*837-112_*837-109deli...
ENST00000686459.1:c.*388-112_*388-109delinsCTTT ENSP00000508909.1:n.*388-112_*388-109deli...
ENST00000688158.1:c.*913-112_*913-109delinsCTTT ENSP00000509254.1:n.*913-112_*913-109deli...
ENST00000688308.1:c.802-112_802-109delinsCTTT ENSP00000508752.1:n.802-112_802-109delins...
ENST00000688922.1:c.723-112_723-109delinsCTTT
ENST00000693560.1:c.1321-112_1321-109delinsCTTT ENSP00000509861.1:n.1321-112_1321-109deli...
ENST00000371953.8:c.802-112_802-109delinsCTTT MANE Select ENSP00000361021.3:n.802-112_802-109delins...
ENST00000371953.7:c.802-112_802-109delinsCTTT ENSP00000361021.3:n.802-112_802-109delins...
ENST00000472832.2:c.229-112_229-109delinsCTTT ENSP00000483066.1:n.229-112_229-109delins...
NM_000314.5:c.802-112_802-109delinsCTTT NP_000305.3:n.802-112_802-109delinsCTTT
NM_000314.6:c.802-112_802-109delinsCTTT NP_000305.3:n.802-112_802-109delinsCTTT
NM_001304717.2:c.1321-112_1321-109delinsCTTT NP_001291646.2:n.1321-112_1321-109delinsC...
NM_001304718.1:c.211-112_211-109delinsCTTT NP_001291647.1:n.211-112_211-109delinsCTT...
XM_006717926.2:c.757-112_757-109delinsCTTT XP_006717989.1:n.757-112_757-109delinsCTT...
XM_011539981.1:c.802-112_802-109delinsCTTT XP_011538283.1:n.802-112_802-109delinsCTT...
XM_011539982.1:c.706-112_706-109delinsCTTT XP_011538284.1:n.706-112_706-109delinsCTT...
XR_945791.1:n.1372-112_1372-109delinsCTTT
NM_000314.7:c.802-112_802-109delinsCTTT NP_000305.3:n.802-112_802-109delinsCTTT
NM_001304717.5:c.1321-112_1321-109delinsCTTT NP_001291646.4:n.1321-112_1321-109delinsC...
NM_001304718.2:c.211-112_211-109delinsCTTT NP_001291647.1:n.211-112_211-109delinsCTT...
NM_000314.8:c.802-112_802-109delinsCTTT MANE Select NP_000305.3:n.802-112_802-109delinsCTTT