Canonical Allele Identifier: CA1926189846

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960809_87960811delinsCAG , CM000672.2:g.87960809_87960811delinsCAG	GRCh38
NC_000010.10:g.89720566_89720568delinsCAG , CM000672.1:g.89720566_89720568delinsCAG	GRCh37
NC_000010.9:g.89710546_89710548delinsCAG	NCBI36
NG_007466.2:g.102371_102373delinsCAG , LRG_311:g.102371_102373delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-85_895-83delinsCAG	ENSP00000514759.2:n.895-85_895-83delinsCA...
ENST00000710265.1:c.802-85_802-83delinsCAG	ENSP00000518161.1:n.802-85_802-83delinsCA...
ENST00000472832.3:c.802-85_802-83delinsCAG	ENSP00000483066.2:n.802-85_802-83delinsCA...
ENST00000688158.2:n.1537-85_1537-83delinsCAG
ENST00000688922.2:c.*632-85_*632-83delinsCAG	ENSP00000508742.2:n.*632-85_*632-83delins...
ENST00000700021.1:c.757-85_757-83delinsCAG	ENSP00000514757.1:n.757-85_757-83delinsCA...
ENST00000700022.1:c.*141-85_*141-83delinsCAG	ENSP00000514758.1:n.*141-85_*141-83delins...
ENST00000700023.1:n.1960-85_1960-83delinsCAG
ENST00000700024.1:n.2194-85_2194-83delinsCAG
ENST00000700025.1:n.1571-85_1571-83delinsCAG
ENST00000700026.1:n.439-85_439-83delinsCAG
ENST00000700029.1:c.729-85_729-83delinsCAG
ENST00000706954.1:c.802-85_802-83delinsCAG	ENSP00000516674.1:n.802-85_802-83delinsCA...
ENST00000706955.1:c.*837-85_*837-83delinsCAG	ENSP00000516675.1:n.*837-85_*837-83delins...
ENST00000686459.1:c.*388-85_*388-83delinsCAG	ENSP00000508909.1:n.*388-85_*388-83delins...
ENST00000688158.1:c.*913-85_*913-83delinsCAG	ENSP00000509254.1:n.*913-85_*913-83delins...
ENST00000688308.1:c.802-85_802-83delinsCAG	ENSP00000508752.1:n.802-85_802-83delinsCA...
ENST00000688922.1:c.723-85_723-83delinsCAG
ENST00000693560.1:c.1321-85_1321-83delinsCAG	ENSP00000509861.1:n.1321-85_1321-83delins...
ENST00000371953.8:c.802-85_802-83delinsCAG MANE Select	ENSP00000361021.3:n.802-85_802-83delinsCA...
ENST00000371953.7:c.802-85_802-83delinsCAG	ENSP00000361021.3:n.802-85_802-83delinsCA...
ENST00000472832.2:c.229-85_229-83delinsCAG	ENSP00000483066.1:n.229-85_229-83delinsCA...
NM_000314.5:c.802-85_802-83delinsCAG	NP_000305.3:n.802-85_802-83delinsCAG
NM_000314.6:c.802-85_802-83delinsCAG	NP_000305.3:n.802-85_802-83delinsCAG
NM_001304717.2:c.1321-85_1321-83delinsCAG	NP_001291646.2:n.1321-85_1321-83delinsCAG...
NM_001304718.1:c.211-85_211-83delinsCAG	NP_001291647.1:n.211-85_211-83delinsCAG
XM_006717926.2:c.757-85_757-83delinsCAG	XP_006717989.1:n.757-85_757-83delinsCAG
XM_011539981.1:c.802-85_802-83delinsCAG	XP_011538283.1:n.802-85_802-83delinsCAG
XM_011539982.1:c.706-85_706-83delinsCAG	XP_011538284.1:n.706-85_706-83delinsCAG
XR_945791.1:n.1372-85_1372-83delinsCAG
NM_000314.7:c.802-85_802-83delinsCAG	NP_000305.3:n.802-85_802-83delinsCAG
NM_001304717.5:c.1321-85_1321-83delinsCAG	NP_001291646.4:n.1321-85_1321-83delinsCAG...
NM_001304718.2:c.211-85_211-83delinsCAG	NP_001291647.1:n.211-85_211-83delinsCAG
NM_000314.8:c.802-85_802-83delinsCAG MANE Select	NP_000305.3:n.802-85_802-83delinsCAG