Canonical Allele Identifier: CA1926189824

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960732_87960734delinsCTT , CM000672.2:g.87960732_87960734delinsCTT	GRCh38
NC_000010.10:g.89720489_89720491delinsCTT , CM000672.1:g.89720489_89720491delinsCTT	GRCh37
NC_000010.9:g.89710469_89710471delinsCTT	NCBI36
NG_007466.2:g.102294_102296delinsCTT , LRG_311:g.102294_102296delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-162_895-160delinsCTT	ENSP00000514759.2:n.895-162_895-160delinsCTT
ENST00000710265.1:c.802-162_802-160delinsCTT	ENSP00000518161.1:n.802-162_802-160delinsCTT
ENST00000472832.3:c.802-162_802-160delinsCTT	ENSP00000483066.2:n.802-162_802-160delinsCTT
ENST00000688158.2:n.1537-162_1537-160delinsCTT
ENST00000688922.2:c.*632-162_*632-160delinsCTT	ENSP00000508742.2:n.*632-162_*632-160delinsCTT
ENST00000700021.1:c.757-162_757-160delinsCTT	ENSP00000514757.1:n.757-162_757-160delinsCTT
ENST00000700022.1:c.*141-162_*141-160delinsCTT	ENSP00000514758.1:n.*141-162_*141-160delinsCTT
ENST00000700023.1:n.1960-162_1960-160delinsCTT
ENST00000700024.1:n.2194-162_2194-160delinsCTT
ENST00000700025.1:n.1571-162_1571-160delinsCTT
ENST00000700026.1:n.439-162_439-160delinsCTT
ENST00000700029.1:c.729-162_729-160delinsCTT
ENST00000706954.1:c.802-162_802-160delinsCTT	ENSP00000516674.1:n.802-162_802-160delinsCTT
ENST00000706955.1:c.*837-162_*837-160delinsCTT	ENSP00000516675.1:n.*837-162_*837-160delinsCTT
ENST00000686459.1:c.*388-162_*388-160delinsCTT	ENSP00000508909.1:n.*388-162_*388-160delinsCTT
ENST00000688158.1:c.*913-162_*913-160delinsCTT	ENSP00000509254.1:n.*913-162_*913-160delinsCTT
ENST00000688308.1:c.802-162_802-160delinsCTT	ENSP00000508752.1:n.802-162_802-160delinsCTT
ENST00000688922.1:c.723-162_723-160delinsCTT
ENST00000693560.1:c.1321-162_1321-160delinsCTT	ENSP00000509861.1:n.1321-162_1321-160delinsCTT
ENST00000371953.8:c.802-162_802-160delinsCTT MANE Select	ENSP00000361021.3:n.802-162_802-160delinsCTT
ENST00000371953.7:c.802-162_802-160delinsCTT	ENSP00000361021.3:n.802-162_802-160delinsCTT
ENST00000472832.2:c.229-162_229-160delinsCTT	ENSP00000483066.1:n.229-162_229-160delinsCTT
NM_000314.5:c.802-162_802-160delinsCTT	NP_000305.3:n.802-162_802-160delinsCTT
NM_000314.6:c.802-162_802-160delinsCTT	NP_000305.3:n.802-162_802-160delinsCTT
NM_001304717.2:c.1321-162_1321-160delinsCTT	NP_001291646.2:n.1321-162_1321-160delinsCTT
NM_001304718.1:c.211-162_211-160delinsCTT	NP_001291647.1:n.211-162_211-160delinsCTT
XM_006717926.2:c.757-162_757-160delinsCTT	XP_006717989.1:n.757-162_757-160delinsCTT
XM_011539981.1:c.802-162_802-160delinsCTT	XP_011538283.1:n.802-162_802-160delinsCTT
XM_011539982.1:c.706-162_706-160delinsCTT	XP_011538284.1:n.706-162_706-160delinsCTT
XR_945791.1:n.1372-162_1372-160delinsCTT
NM_000314.7:c.802-162_802-160delinsCTT	NP_000305.3:n.802-162_802-160delinsCTT
NM_001304717.5:c.1321-162_1321-160delinsCTT	NP_001291646.4:n.1321-162_1321-160delinsCTT
NM_001304718.2:c.211-162_211-160delinsCTT	NP_001291647.1:n.211-162_211-160delinsCTT
NM_000314.8:c.802-162_802-160delinsCTT MANE Select	NP_000305.3:n.802-162_802-160delinsCTT