Canonical Allele Identifier: CA470973988

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720767A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961010A>C , CM000672.2:g.87961010A>C	GRCh38
NC_000010.10:g.89720767A>C , CM000672.1:g.89720767A>C	GRCh37
NC_000010.9:g.89710747A>C	NCBI36
NG_007466.2:g.102572A>C , LRG_311:g.102572A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1011A>C	ENSP00000514759.2:p.Ile337=
ENST00000710265.1:c.918A>C	ENSP00000518161.1:p.Ile306=
ENST00000472832.3:c.918A>C	ENSP00000483066.2:p.Ile306=
ENST00000688158.2:n.1653A>C
ENST00000688922.2:c.*748A>C	ENSP00000508742.2:n.*748A>C
ENST00000700021.1:c.873A>C	ENSP00000514757.1:p.Ile291=
ENST00000700022.1:c.*257A>C	ENSP00000514758.1:n.*257A>C
ENST00000700023.1:n.2076A>C
ENST00000700024.1:n.2310A>C
ENST00000700025.1:n.1687A>C
ENST00000700026.1:n.555A>C
ENST00000706954.1:c.918A>C	ENSP00000516674.1:p.Ile306=
ENST00000706955.1:c.*953A>C	ENSP00000516675.1:n.*953A>C
ENST00000686459.1:c.*504A>C	ENSP00000508909.1:n.*504A>C
ENST00000688158.1:c.*1029A>C	ENSP00000509254.1:n.*1029A>C
ENST00000688308.1:c.918A>C	ENSP00000508752.1:p.Ile306=
ENST00000688922.1:c.839A>C
ENST00000693560.1:c.1437A>C	ENSP00000509861.1:p.Ile479=
ENST00000371953.8:c.918A>C MANE Select	ENSP00000361021.3:p.Ile306=
ENST00000371953.7:c.918A>C	ENSP00000361021.3:p.Ile306=
ENST00000472832.2:c.345A>C	ENSP00000483066.1:p.Ile115=
NM_000314.5:c.918A>C	NP_000305.3:p.Ile306=
NM_000314.6:c.918A>C	NP_000305.3:p.Ile306=
NM_001304717.2:c.1437A>C	NP_001291646.2:p.Ile479=
NM_001304718.1:c.327A>C	NP_001291647.1:p.Ile109=
XM_006717926.2:c.873A>C	XP_006717989.1:p.Ile291=
XM_011539981.1:c.918A>C	XP_011538283.1:p.Ile306=
XM_011539982.1:c.822A>C	XP_011538284.1:p.Ile274=
XR_945791.1:n.1488A>C
NM_000314.7:c.918A>C	NP_000305.3:p.Ile306=
NM_001304717.5:c.1437A>C	NP_001291646.4:p.Ile479=
NM_001304718.2:c.327A>C	NP_001291647.1:p.Ile109=
NM_000314.8:c.918A>C MANE Select	NP_000305.3:p.Ile306=