Canonical Allele Identifier: CA930924171

Gene: PTEN

Linked Data

• gnomAD v3: 10-87960893-G-GTTT
• gnomAD v4: 10-87960893-G-GTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960893_87960894insTTT , CM000672.2:g.87960893_87960894insTTT	GRCh38
NC_000010.10:g.89720650_89720651insTTT , CM000672.1:g.89720650_89720651insTTT	GRCh37
NC_000010.9:g.89710630_89710631insTTT	NCBI36
NG_007466.2:g.102455_102456insTTT , LRG_311:g.102455_102456insTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-1_895insTTT	ENSP00000514759.2:n.895-1_895insTTT
ENST00000710265.1:c.802-1_802insTTT	ENSP00000518161.1:n.802-1_802insTTT
ENST00000472832.3:c.802-1_802insTTT	ENSP00000483066.2:n.802-1_802insTTT
ENST00000688158.2:n.1537-1_1537insTTT
ENST00000688922.2:c.*632-1_*632insTTT	ENSP00000508742.2:n.*632-1_*632insTTT
ENST00000700021.1:c.757-1_757insTTT	ENSP00000514757.1:n.757-1_757insTTT
ENST00000700022.1:c.*141-1_*141insTTT	ENSP00000514758.1:n.*141-1_*141insTTT
ENST00000700023.1:n.1960-1_1960insTTT
ENST00000700024.1:n.2194-1_2194insTTT
ENST00000700025.1:n.1571-1_1571insTTT
ENST00000700026.1:n.439-1_439insTTT
ENST00000700029.1:c.729-1_729insTTT
ENST00000706954.1:c.802-1_802insTTT	ENSP00000516674.1:n.802-1_802insTTT
ENST00000706955.1:c.*837-1_*837insTTT	ENSP00000516675.1:n.*837-1_*837insTTT
ENST00000686459.1:c.*388-1_*388insTTT	ENSP00000508909.1:n.*388-1_*388insTTT
ENST00000688158.1:c.*913-1_*913insTTT	ENSP00000509254.1:n.*913-1_*913insTTT
ENST00000688308.1:c.802-1_802insTTT	ENSP00000508752.1:n.802-1_802insTTT
ENST00000688922.1:c.723-1_723insTTT
ENST00000693560.1:c.1321-1_1321insTTT	ENSP00000509861.1:n.1321-1_1321insTTT
ENST00000371953.8:c.802-1_802insTTT MANE Select	ENSP00000361021.3:n.802-1_802insTTT
ENST00000371953.7:c.802-1_802insTTT	ENSP00000361021.3:n.802-1_802insTTT
ENST00000472832.2:c.229-1_229insTTT	ENSP00000483066.1:n.229-1_229insTTT
NM_000314.5:c.802-1_802insTTT	NP_000305.3:n.802-1_802insTTT
NM_000314.6:c.802-1_802insTTT	NP_000305.3:n.802-1_802insTTT
NM_001304717.2:c.1321-1_1321insTTT	NP_001291646.2:n.1321-1_1321insTTT
NM_001304718.1:c.211-1_211insTTT	NP_001291647.1:n.211-1_211insTTT
XM_006717926.2:c.757-1_757insTTT	XP_006717989.1:n.757-1_757insTTT
XM_011539981.1:c.802-1_802insTTT	XP_011538283.1:n.802-1_802insTTT
XM_011539982.1:c.706-1_706insTTT	XP_011538284.1:n.706-1_706insTTT
XR_945791.1:n.1372-1_1372insTTT
NM_000314.7:c.802-1_802insTTT	NP_000305.3:n.802-1_802insTTT
NM_001304717.5:c.1321-1_1321insTTT	NP_001291646.4:n.1321-1_1321insTTT
NM_001304718.2:c.211-1_211insTTT	NP_001291647.1:n.211-1_211insTTT
NM_000314.8:c.802-1_802insTTT MANE Select	NP_000305.3:n.802-1_802insTTT