Canonical Allele Identifier: CA2610047675

Gene: PTEN

Linked Data

• gnomAD v4: 10-87960865-C-CTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960870_87960871insTTTTTT , CM000672.2:g.87960870_87960871insTTTTTT	GRCh38
NC_000010.10:g.89720627_89720628insTTTTTT , CM000672.1:g.89720627_89720628insTTTTTT	GRCh37
NC_000010.9:g.89710607_89710608insTTTTTT	NCBI36
NG_007466.2:g.102432_102433insTTTTTT , LRG_311:g.102432_102433insTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.895-24_895-23insTTTTTT	ENSP00000514759.2:n.895-24_895-23insTTTTTT
ENST00000710265.1:c.802-24_802-23insTTTTTT	ENSP00000518161.1:n.802-24_802-23insTTTTTT
ENST00000472832.3:c.802-24_802-23insTTTTTT	ENSP00000483066.2:n.802-24_802-23insTTTTTT
ENST00000688158.2:n.1537-24_1537-23insTTTTTT
ENST00000688922.2:c.*632-24_*632-23insTTTTTT	ENSP00000508742.2:n.*632-24_*632-23insTTTTTT
ENST00000700021.1:c.757-24_757-23insTTTTTT	ENSP00000514757.1:n.757-24_757-23insTTTTTT
ENST00000700022.1:c.*141-24_*141-23insTTTTTT	ENSP00000514758.1:n.*141-24_*141-23insTTTTTT
ENST00000700023.1:n.1960-24_1960-23insTTTTTT
ENST00000700024.1:n.2194-24_2194-23insTTTTTT
ENST00000700025.1:n.1571-24_1571-23insTTTTTT
ENST00000700026.1:n.439-24_439-23insTTTTTT
ENST00000700029.1:c.729-24_729-23insTTTTTT
ENST00000706954.1:c.802-24_802-23insTTTTTT	ENSP00000516674.1:n.802-24_802-23insTTTTTT
ENST00000706955.1:c.*837-24_*837-23insTTTTTT	ENSP00000516675.1:n.*837-24_*837-23insTTTTTT
ENST00000686459.1:c.*388-24_*388-23insTTTTTT	ENSP00000508909.1:n.*388-24_*388-23insTTTTTT
ENST00000688158.1:c.*913-24_*913-23insTTTTTT	ENSP00000509254.1:n.*913-24_*913-23insTTTTTT
ENST00000688308.1:c.802-24_802-23insTTTTTT	ENSP00000508752.1:n.802-24_802-23insTTTTTT
ENST00000688922.1:c.723-24_723-23insTTTTTT
ENST00000693560.1:c.1321-24_1321-23insTTTTTT	ENSP00000509861.1:n.1321-24_1321-23insTTTTTT
ENST00000371953.8:c.802-24_802-23insTTTTTT MANE Select	ENSP00000361021.3:n.802-24_802-23insTTTTTT
ENST00000371953.7:c.802-24_802-23insTTTTTT	ENSP00000361021.3:n.802-24_802-23insTTTTTT
ENST00000472832.2:c.229-24_229-23insTTTTTT	ENSP00000483066.1:n.229-24_229-23insTTTTTT
NM_000314.5:c.802-24_802-23insTTTTTT	NP_000305.3:n.802-24_802-23insTTTTTT
NM_000314.6:c.802-24_802-23insTTTTTT	NP_000305.3:n.802-24_802-23insTTTTTT
NM_001304717.2:c.1321-24_1321-23insTTTTTT	NP_001291646.2:n.1321-24_1321-23insTTTTTT
NM_001304718.1:c.211-24_211-23insTTTTTT	NP_001291647.1:n.211-24_211-23insTTTTTT
XM_006717926.2:c.757-24_757-23insTTTTTT	XP_006717989.1:n.757-24_757-23insTTTTTT
XM_011539981.1:c.802-24_802-23insTTTTTT	XP_011538283.1:n.802-24_802-23insTTTTTT
XM_011539982.1:c.706-24_706-23insTTTTTT	XP_011538284.1:n.706-24_706-23insTTTTTT
XR_945791.1:n.1372-24_1372-23insTTTTTT
NM_000314.7:c.802-24_802-23insTTTTTT	NP_000305.3:n.802-24_802-23insTTTTTT
NM_001304717.5:c.1321-24_1321-23insTTTTTT	NP_001291646.4:n.1321-24_1321-23insTTTTTT
NM_001304718.2:c.211-24_211-23insTTTTTT	NP_001291647.1:n.211-24_211-23insTTTTTT
NM_000314.8:c.802-24_802-23insTTTTTT MANE Select	NP_000305.3:n.802-24_802-23insTTTTTT