Canonical Allele Identifier: CA1926189945

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960902G= , CM000672.2:g.87960902G=	GRCh38
NC_000010.10:g.89720659G= , CM000672.1:g.89720659G=	GRCh37
NC_000010.9:g.89710639G=	NCBI36
NG_007466.2:g.102464G= , LRG_311:g.102464G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.903G=	ENSP00000514759.2:p.Met301=
ENST00000710265.1:c.810G=	ENSP00000518161.1:p.Met270=
ENST00000472832.3:c.810G=	ENSP00000483066.2:p.Met270=
ENST00000688158.2:n.1545G=
ENST00000688922.2:c.*640G=	ENSP00000508742.2:n.*640G=
ENST00000700021.1:c.765G=	ENSP00000514757.1:p.Met255=
ENST00000700022.1:c.*149G=	ENSP00000514758.1:n.*149G=
ENST00000700023.1:n.1968G=
ENST00000700024.1:n.2202G=
ENST00000700025.1:n.1579G=
ENST00000700026.1:n.447G=
ENST00000700029.1:c.737G=
ENST00000706954.1:c.810G=	ENSP00000516674.1:p.Met270=
ENST00000706955.1:c.*845G=	ENSP00000516675.1:n.*845G=
ENST00000686459.1:c.*396G=	ENSP00000508909.1:n.*396G=
ENST00000688158.1:c.*921G=	ENSP00000509254.1:n.*921G=
ENST00000688308.1:c.810G=	ENSP00000508752.1:p.Met270=
ENST00000688922.1:c.731G=
ENST00000693560.1:c.1329G=	ENSP00000509861.1:p.Met443=
ENST00000371953.8:c.810G= MANE Select	ENSP00000361021.3:p.Met270=
ENST00000371953.7:c.810G=	ENSP00000361021.3:p.Met270=
ENST00000472832.2:c.237G=	ENSP00000483066.1:p.Met79=
NM_000314.5:c.810G=	NP_000305.3:p.Met270=
NM_000314.6:c.810G=	NP_000305.3:p.Met270=
NM_001304717.2:c.1329G=	NP_001291646.2:p.Met443=
NM_001304718.1:c.219G=	NP_001291647.1:p.Met73=
XM_006717926.2:c.765G=	XP_006717989.1:p.Met255=
XM_011539981.1:c.810G=	XP_011538283.1:p.Met270=
XM_011539982.1:c.714G=	XP_011538284.1:p.Met238=
XR_945791.1:n.1380G=
NM_000314.7:c.810G=	NP_000305.3:p.Met270=
NM_001304717.5:c.1329G=	NP_001291646.4:p.Met443=
NM_001304718.2:c.219G=	NP_001291647.1:p.Met73=
NM_000314.8:c.810G= MANE Select	NP_000305.3:p.Met270=