Canonical Allele Identifier: CA1926173928

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965375A= , CM000672.2:g.87965375A=	GRCh38
NC_000010.10:g.89725132A= , CM000672.1:g.89725132A=	GRCh37
NC_000010.9:g.89715112A=	NCBI36
NG_007466.2:g.106937A= , LRG_311:g.106937A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1208A=	ENSP00000514759.2:p.Asn403=
ENST00000710265.1:c.*144A=	ENSP00000518161.1:n.*144A=
ENST00000688158.2:n.1850A=
ENST00000688922.2:c.*945A=	ENSP00000508742.2:n.*945A=
ENST00000700021.1:c.1070A=	ENSP00000514757.1:p.Asn357=
ENST00000700022.1:c.*454A=	ENSP00000514758.1:n.*454A=
ENST00000700023.1:n.2273A=
ENST00000700024.1:n.2507A=
ENST00000706954.1:c.1115A=	ENSP00000516674.1:p.Asn372=
ENST00000706955.1:c.*1150A=	ENSP00000516675.1:n.*1150A=
ENST00000686459.1:c.*701A=	ENSP00000508909.1:n.*701A=
ENST00000688158.1:c.*1226A=	ENSP00000509254.1:n.*1226A=
ENST00000688308.1:c.1115A=	ENSP00000508752.1:p.Asn372=
ENST00000688922.1:c.1036A=
ENST00000693560.1:c.1634A=	ENSP00000509861.1:p.Asn545=
ENST00000371953.8:c.1115A= MANE Select	ENSP00000361021.3:p.Asn372=
ENST00000371953.7:c.1115A=	ENSP00000361021.3:p.Asn372=
NM_000314.5:c.1115A=	NP_000305.3:p.Asn372=
NM_000314.6:c.1115A=	NP_000305.3:p.Asn372=
NM_001304717.2:c.1634A=	NP_001291646.2:p.Asn545=
NM_001304718.1:c.524A=	NP_001291647.1:p.Asn175=
XM_006717926.2:c.1070A=	XP_006717989.1:p.Asn357=
XM_011539982.1:c.1019A=	XP_011538284.1:p.Asn340=
XR_945791.1:n.1685A=
NM_000314.7:c.1115A=	NP_000305.3:p.Asn372=
NM_001304717.5:c.1634A=	NP_001291646.4:p.Asn545=
NM_001304718.2:c.524A=	NP_001291647.1:p.Asn175=
NM_000314.8:c.1115A= MANE Select	NP_000305.3:p.Asn372=