Canonical Allele Identifier: CA1926182373

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952138G= , CM000672.2:g.87952138G=	GRCh38
NC_000010.10:g.89711895G= , CM000672.1:g.89711895G=	GRCh37
NC_000010.9:g.89701875G=	NCBI36
NG_007466.2:g.93700G= , LRG_311:g.93700G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.513G=	ENSP00000514759.2:p.Gln171=
ENST00000710265.1:c.513G=	ENSP00000518161.1:p.Gln171=
ENST00000472832.3:c.513G=	ENSP00000483066.2:p.Gln171=
ENST00000688158.2:n.1248G=
ENST00000688922.2:c.*343G=	ENSP00000508742.2:n.*343G=
ENST00000700021.1:c.468G=	ENSP00000514757.1:p.Gln156=
ENST00000700022.1:c.493-5715G=	ENSP00000514758.1:n.493-5715G=
ENST00000700023.1:n.1671G=
ENST00000700024.1:n.1905G=
ENST00000700025.1:n.1282G=
ENST00000700029.1:c.347G=
ENST00000706954.1:c.513G=	ENSP00000516674.1:p.Gln171=
ENST00000706955.1:c.*548G=	ENSP00000516675.1:n.*548G=
ENST00000686459.1:c.*99G=	ENSP00000508909.1:n.*99G=
ENST00000688158.1:c.*624G=	ENSP00000509254.1:n.*624G=
ENST00000688308.1:c.513G=	ENSP00000508752.1:p.Gln171=
ENST00000688922.1:c.434G=
ENST00000693560.1:c.1032G=	ENSP00000509861.1:p.Gln344=
ENST00000371953.8:c.513G= MANE Select	ENSP00000361021.3:p.Gln171=
ENST00000371953.7:c.513G=	ENSP00000361021.3:p.Gln171=
NM_000314.5:c.513G=	NP_000305.3:p.Gln171=
NM_000314.6:c.513G=	NP_000305.3:p.Gln171=
NM_001304717.2:c.1032G=	NP_001291646.2:p.Gln344=
NM_001304718.1:c.-79G=	NP_001291647.1:n.-79G=
XM_006717926.2:c.468G=	XP_006717989.1:p.Gln156=
XM_011539981.1:c.513G=	XP_011538283.1:p.Gln171=
XM_011539982.1:c.417G=	XP_011538284.1:p.Gln139=
XR_945789.1:n.1384G=
XR_945790.1:n.1501G=
XR_945791.1:n.1205-5715G=
NM_000314.7:c.513G=	NP_000305.3:p.Gln171=
NM_001304717.5:c.1032G=	NP_001291646.4:p.Gln344=
NM_001304718.2:c.-79G=	NP_001291647.1:n.-79G=
NM_000314.8:c.513G= MANE Select	NP_000305.3:p.Gln171=