Canonical Allele Identifier: CA2579927194

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87864483_87864484delinsAT , CM000672.2:g.87864483_87864484delinsAT	GRCh38
NC_000010.10:g.89624240_89624241delinsAT , CM000672.1:g.89624240_89624241delinsAT	GRCh37
NC_000010.9:g.89614220_89614221delinsAT	NCBI36
NG_007466.2:g.6045_6046delinsAT , LRG_311:g.6045_6046delinsAT
NG_033079.1:g.3954_3955delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.14_15delinsAT	ENSP00000514759.2:p.Ile5Asn
ENST00000710265.1:c.14_15delinsAT	ENSP00000518161.1:p.Ile5Asn
ENST00000472832.3:c.14_15delinsAT	ENSP00000483066.2:p.Ile5Asn
ENST00000688922.2:c.14_15delinsAT	ENSP00000508742.2:p.Ile5Asn
ENST00000700021.1:c.14_15delinsAT	ENSP00000514757.1:p.Ile5Asn
ENST00000700022.1:c.14_15delinsAT	ENSP00000514758.1:p.Ile5Asn
ENST00000706954.1:c.14_15delinsAT	ENSP00000516674.1:p.Ile5Asn
ENST00000706955.1:c.14_15delinsAT	ENSP00000516675.1:p.Ile5Asn
ENST00000686459.1:c.14_15delinsAT	ENSP00000508909.1:p.Ile5Asn
ENST00000688158.1:c.14_15delinsAT	ENSP00000509254.1:p.Ile5Asn
ENST00000688308.1:c.14_15delinsAT	ENSP00000508752.1:p.Ile5Asn
ENST00000693560.1:c.533_534delinsAT	ENSP00000509861.1:p.Ile178Asn
ENST00000371953.8:c.14_15delinsAT MANE Select	ENSP00000361021.3:p.Ile5Asn
ENST00000371953.7:c.14_15delinsAT	ENSP00000361021.3:p.Ile5Asn
ENST00000462694.1:n.16_17delinsAT
ENST00000487939.1:n.35_36delinsAT
ENST00000610634.1:c.-89_-88delinsAT	ENSP00000477517.1:n.-89_-88delinsAT
NM_000314.5:c.14_15delinsAT	NP_000305.3:p.Ile5Asn
NM_000314.6:c.14_15delinsAT	NP_000305.3:p.Ile5Asn
NM_001304717.2:c.533_534delinsAT	NP_001291646.2:p.Ile178Asn
NM_001304718.1:c.-692_-691delinsAT	NP_001291647.1:n.-692_-691delinsAT
XM_006717926.2:c.14_15delinsAT	XP_006717989.1:p.Ile5Asn
XM_011539981.1:c.14_15delinsAT	XP_011538283.1:p.Ile5Asn
XR_945789.1:n.726_727delinsAT
XR_945790.1:n.726_727delinsAT
XR_945791.1:n.726_727delinsAT
NM_000314.7:c.14_15delinsAT	NP_000305.3:p.Ile5Asn
NM_001304717.5:c.533_534delinsAT	NP_001291646.4:p.Ile178Asn
NM_001304718.2:c.-692_-691delinsAT	NP_001291647.1:n.-692_-691delinsAT
NM_000314.8:c.14_15delinsAT MANE Select	NP_000305.3:p.Ile5Asn