Canonical Allele Identifier: CA470973934

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720695A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960938A>C , CM000672.2:g.87960938A>C	GRCh38
NC_000010.10:g.89720695A>C , CM000672.1:g.89720695A>C	GRCh37
NC_000010.9:g.89710675A>C	NCBI36
NG_007466.2:g.102500A>C , LRG_311:g.102500A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.939A>C	ENSP00000514759.2:p.Gly313=
ENST00000710265.1:c.846A>C	ENSP00000518161.1:p.Gly282=
ENST00000472832.3:c.846A>C	ENSP00000483066.2:p.Gly282=
ENST00000688158.2:n.1581A>C
ENST00000688922.2:c.*676A>C	ENSP00000508742.2:n.*676A>C
ENST00000700021.1:c.801A>C	ENSP00000514757.1:p.Gly267=
ENST00000700022.1:c.*185A>C	ENSP00000514758.1:n.*185A>C
ENST00000700023.1:n.2004A>C
ENST00000700024.1:n.2238A>C
ENST00000700025.1:n.1615A>C
ENST00000700026.1:n.483A>C
ENST00000700029.1:c.773A>C
ENST00000706954.1:c.846A>C	ENSP00000516674.1:p.Gly282=
ENST00000706955.1:c.*881A>C	ENSP00000516675.1:n.*881A>C
ENST00000686459.1:c.*432A>C	ENSP00000508909.1:n.*432A>C
ENST00000688158.1:c.*957A>C	ENSP00000509254.1:n.*957A>C
ENST00000688308.1:c.846A>C	ENSP00000508752.1:p.Gly282=
ENST00000688922.1:c.767A>C
ENST00000693560.1:c.1365A>C	ENSP00000509861.1:p.Gly455=
ENST00000371953.8:c.846A>C MANE Select	ENSP00000361021.3:p.Gly282=
ENST00000371953.7:c.846A>C	ENSP00000361021.3:p.Gly282=
ENST00000472832.2:c.273A>C	ENSP00000483066.1:p.Gly91=
NM_000314.5:c.846A>C	NP_000305.3:p.Gly282=
NM_000314.6:c.846A>C	NP_000305.3:p.Gly282=
NM_001304717.2:c.1365A>C	NP_001291646.2:p.Gly455=
NM_001304718.1:c.255A>C	NP_001291647.1:p.Gly85=
XM_006717926.2:c.801A>C	XP_006717989.1:p.Gly267=
XM_011539981.1:c.846A>C	XP_011538283.1:p.Gly282=
XM_011539982.1:c.750A>C	XP_011538284.1:p.Gly250=
XR_945791.1:n.1416A>C
NM_000314.7:c.846A>C	NP_000305.3:p.Gly282=
NM_001304717.5:c.1365A>C	NP_001291646.4:p.Gly455=
NM_001304718.2:c.255A>C	NP_001291647.1:p.Gly85=
NM_000314.8:c.846A>C MANE Select	NP_000305.3:p.Gly282=