Canonical Allele Identifier: CA891834572

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894033_87894035delinsTGG , CM000672.2:g.87894033_87894035delinsTGG	GRCh38
NC_000010.10:g.89653790_89653792delinsTGG , CM000672.1:g.89653790_89653792delinsTGG	GRCh37
NC_000010.9:g.89643770_89643772delinsTGG	NCBI36
NG_007466.2:g.35595_35597delinsTGG , LRG_311:g.35595_35597delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.88_90delinsTGG	ENSP00000514759.2:p.Pro30Trp
ENST00000710265.1:c.88_90delinsTGG	ENSP00000518161.1:p.Pro30Trp
ENST00000472832.3:c.88_90delinsTGG	ENSP00000483066.2:p.Pro30Trp
ENST00000688158.2:n.899+13595_899+13597delinsTGG
ENST00000688922.2:c.88_90delinsTGG	ENSP00000508742.2:p.Pro30Trp
ENST00000700021.1:c.88_90delinsTGG	ENSP00000514757.1:p.Pro30Trp
ENST00000700022.1:c.88_90delinsTGG	ENSP00000514758.1:p.Pro30Trp
ENST00000706954.1:c.88_90delinsTGG	ENSP00000516674.1:p.Pro30Trp
ENST00000706955.1:c.*123_*125delinsTGG	ENSP00000516675.1:n.*123_*125delinsTGG
ENST00000686459.1:c.88_90delinsTGG	ENSP00000508909.1:p.Pro30Trp
ENST00000688158.1:c.*275+13595_*275+13597delinsTGG	ENSP00000509254.1:n.*275+13595_*275+13597delinsTGG
ENST00000688308.1:c.88_90delinsTGG	ENSP00000508752.1:p.Pro30Trp
ENST00000693560.1:c.607_609delinsTGG	ENSP00000509861.1:p.Pro203Trp
ENST00000371953.8:c.88_90delinsTGG MANE Select	ENSP00000361021.3:p.Pro30Trp
ENST00000371953.7:c.88_90delinsTGG	ENSP00000361021.3:p.Pro30Trp
ENST00000462694.1:n.90_92delinsTGG
ENST00000610634.1:c.-15_-13delinsTGG	ENSP00000477517.1:n.-15_-13delinsTGG
NM_000314.5:c.88_90delinsTGG	NP_000305.3:p.Pro30Trp
NM_000314.6:c.88_90delinsTGG	NP_000305.3:p.Pro30Trp
NM_001304717.2:c.607_609delinsTGG	NP_001291646.2:p.Pro203Trp
NM_001304718.1:c.-618_-616delinsTGG	NP_001291647.1:n.-618_-616delinsTGG
XM_006717926.2:c.88_90delinsTGG	XP_006717989.1:p.Pro30Trp
XM_011539981.1:c.88_90delinsTGG	XP_011538283.1:p.Pro30Trp
XM_011539982.1:c.68+13595_68+13597delinsTGG	XP_011538284.1:n.68+13595_68+13597delinsTGG
XR_945789.1:n.800_802delinsTGG
XR_945790.1:n.800_802delinsTGG
XR_945791.1:n.800_802delinsTGG
NM_000314.7:c.88_90delinsTGG	NP_000305.3:p.Pro30Trp
NM_001304717.5:c.607_609delinsTGG	NP_001291646.4:p.Pro203Trp
NM_001304718.2:c.-618_-616delinsTGG	NP_001291647.1:n.-618_-616delinsTGG
NM_000314.8:c.88_90delinsTGG MANE Select	NP_000305.3:p.Pro30Trp