Canonical Allele Identifier: CA470670799

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725052G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965295G>T , CM000672.2:g.87965295G>T	GRCh38
NC_000010.10:g.89725052G>T , CM000672.1:g.89725052G>T	GRCh37
NC_000010.9:g.89715032G>T	NCBI36
NG_007466.2:g.106857G>T , LRG_311:g.106857G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1128G>T	ENSP00000514759.2:p.Leu376=
ENST00000710265.1:c.*64G>T	ENSP00000518161.1:n.*64G>T
ENST00000688158.2:n.1770G>T
ENST00000688922.2:c.*865G>T	ENSP00000508742.2:n.*865G>T
ENST00000700021.1:c.990G>T	ENSP00000514757.1:p.Leu330=
ENST00000700022.1:c.*374G>T	ENSP00000514758.1:n.*374G>T
ENST00000700023.1:n.2193G>T
ENST00000700024.1:n.2427G>T
ENST00000706954.1:c.1035G>T	ENSP00000516674.1:p.Leu345=
ENST00000706955.1:c.*1070G>T	ENSP00000516675.1:n.*1070G>T
ENST00000686459.1:c.*621G>T	ENSP00000508909.1:n.*621G>T
ENST00000688158.1:c.*1146G>T	ENSP00000509254.1:n.*1146G>T
ENST00000688308.1:c.1035G>T	ENSP00000508752.1:p.Leu345=
ENST00000688922.1:c.956G>T
ENST00000693560.1:c.1554G>T	ENSP00000509861.1:p.Leu518=
ENST00000371953.8:c.1035G>T MANE Select	ENSP00000361021.3:p.Leu345=
ENST00000371953.7:c.1035G>T	ENSP00000361021.3:p.Leu345=
NM_000314.5:c.1035G>T	NP_000305.3:p.Leu345=
NM_000314.6:c.1035G>T	NP_000305.3:p.Leu345=
NM_001304717.2:c.1554G>T	NP_001291646.2:p.Leu518=
NM_001304718.1:c.444G>T	NP_001291647.1:p.Leu148=
XM_006717926.2:c.990G>T	XP_006717989.1:p.Leu330=
XM_011539982.1:c.939G>T	XP_011538284.1:p.Leu313=
XR_945791.1:n.1605G>T
NM_000314.7:c.1035G>T	NP_000305.3:p.Leu345=
NM_001304717.5:c.1554G>T	NP_001291646.4:p.Leu518=
NM_001304718.2:c.444G>T	NP_001291647.1:p.Leu148=
NM_000314.8:c.1035G>T MANE Select	NP_000305.3:p.Leu345=