Canonical Allele Identifier: CA2610047707

Gene: PTEN

Linked Data

• gnomAD v4: 10-87960871-C-CTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960875_87960876insTTTTTTTT , CM000672.2:g.87960875_87960876insTTTTTTTT	GRCh38
NC_000010.10:g.89720632_89720633insTTTTTTTT , CM000672.1:g.89720632_89720633insTTTTTTTT	GRCh37
NC_000010.9:g.89710612_89710613insTTTTTTTT	NCBI36
NG_007466.2:g.102437_102438insTTTTTTTT , LRG_311:g.102437_102438insTTTTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-19_895-18insTTTTTTTT	ENSP00000514759.2:n.895-19_895-18insTTTTTTTT
ENST00000710265.1:c.802-19_802-18insTTTTTTTT	ENSP00000518161.1:n.802-19_802-18insTTTTTTTT
ENST00000472832.3:c.802-19_802-18insTTTTTTTT	ENSP00000483066.2:n.802-19_802-18insTTTTTTTT
ENST00000688158.2:n.1537-19_1537-18insTTTTTTTT
ENST00000688922.2:c.*632-19_*632-18insTTTTTTTT	ENSP00000508742.2:n.*632-19_*632-18insTTTTTTTT
ENST00000700021.1:c.757-19_757-18insTTTTTTTT	ENSP00000514757.1:n.757-19_757-18insTTTTTTTT
ENST00000700022.1:c.*141-19_*141-18insTTTTTTTT	ENSP00000514758.1:n.*141-19_*141-18insTTTTTTTT
ENST00000700023.1:n.1960-19_1960-18insTTTTTTTT
ENST00000700024.1:n.2194-19_2194-18insTTTTTTTT
ENST00000700025.1:n.1571-19_1571-18insTTTTTTTT
ENST00000700026.1:n.439-19_439-18insTTTTTTTT
ENST00000700029.1:c.729-19_729-18insTTTTTTTT
ENST00000706954.1:c.802-19_802-18insTTTTTTTT	ENSP00000516674.1:n.802-19_802-18insTTTTTTTT
ENST00000706955.1:c.*837-19_*837-18insTTTTTTTT	ENSP00000516675.1:n.*837-19_*837-18insTTTTTTTT
ENST00000686459.1:c.*388-19_*388-18insTTTTTTTT	ENSP00000508909.1:n.*388-19_*388-18insTTTTTTTT
ENST00000688158.1:c.*913-19_*913-18insTTTTTTTT	ENSP00000509254.1:n.*913-19_*913-18insTTTTTTTT
ENST00000688308.1:c.802-19_802-18insTTTTTTTT	ENSP00000508752.1:n.802-19_802-18insTTTTTTTT
ENST00000688922.1:c.723-19_723-18insTTTTTTTT
ENST00000693560.1:c.1321-19_1321-18insTTTTTTTT	ENSP00000509861.1:n.1321-19_1321-18insTTTTTTTT
ENST00000371953.8:c.802-19_802-18insTTTTTTTT MANE Select	ENSP00000361021.3:n.802-19_802-18insTTTTTTTT
ENST00000371953.7:c.802-19_802-18insTTTTTTTT	ENSP00000361021.3:n.802-19_802-18insTTTTTTTT
ENST00000472832.2:c.229-19_229-18insTTTTTTTT	ENSP00000483066.1:n.229-19_229-18insTTTTTTTT
NM_000314.5:c.802-19_802-18insTTTTTTTT	NP_000305.3:n.802-19_802-18insTTTTTTTT
NM_000314.6:c.802-19_802-18insTTTTTTTT	NP_000305.3:n.802-19_802-18insTTTTTTTT
NM_001304717.2:c.1321-19_1321-18insTTTTTTTT	NP_001291646.2:n.1321-19_1321-18insTTTTTTTT
NM_001304718.1:c.211-19_211-18insTTTTTTTT	NP_001291647.1:n.211-19_211-18insTTTTTTTT
XM_006717926.2:c.757-19_757-18insTTTTTTTT	XP_006717989.1:n.757-19_757-18insTTTTTTTT
XM_011539981.1:c.802-19_802-18insTTTTTTTT	XP_011538283.1:n.802-19_802-18insTTTTTTTT
XM_011539982.1:c.706-19_706-18insTTTTTTTT	XP_011538284.1:n.706-19_706-18insTTTTTTTT
XR_945791.1:n.1372-19_1372-18insTTTTTTTT
NM_000314.7:c.802-19_802-18insTTTTTTTT	NP_000305.3:n.802-19_802-18insTTTTTTTT
NM_001304717.5:c.1321-19_1321-18insTTTTTTTT	NP_001291646.4:n.1321-19_1321-18insTTTTTTTT
NM_001304718.2:c.211-19_211-18insTTTTTTTT	NP_001291647.1:n.211-19_211-18insTTTTTTTT
NM_000314.8:c.802-19_802-18insTTTTTTTT MANE Select	NP_000305.3:n.802-19_802-18insTTTTTTTT