Canonical Allele Identifier: CA470671447

Gene: PTEN

Linked Data

• dbSNP Id: rs2132290039
• MyVariant Identifiers: chr10:g.89725163C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965406C>G , CM000672.2:g.87965406C>G	GRCh38
NC_000010.10:g.89725163C>G , CM000672.1:g.89725163C>G	GRCh37
NC_000010.9:g.89715143C>G	NCBI36
NG_007466.2:g.106968C>G , LRG_311:g.106968C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1239C>G	ENSP00000514759.2:p.Thr413=
ENST00000710265.1:c.*175C>G	ENSP00000518161.1:n.*175C>G
ENST00000688158.2:n.1881C>G
ENST00000688922.2:c.*976C>G	ENSP00000508742.2:n.*976C>G
ENST00000700021.1:c.1101C>G	ENSP00000514757.1:p.Thr367=
ENST00000700022.1:c.*485C>G	ENSP00000514758.1:n.*485C>G
ENST00000700023.1:n.2304C>G
ENST00000700024.1:n.2538C>G
ENST00000706954.1:c.1146C>G	ENSP00000516674.1:p.Thr382=
ENST00000706955.1:c.*1181C>G	ENSP00000516675.1:n.*1181C>G
ENST00000686459.1:c.*732C>G	ENSP00000508909.1:n.*732C>G
ENST00000688158.1:c.*1257C>G	ENSP00000509254.1:n.*1257C>G
ENST00000688308.1:c.1146C>G	ENSP00000508752.1:p.Thr382=
ENST00000688922.1:c.1067C>G
ENST00000693560.1:c.1665C>G	ENSP00000509861.1:p.Thr555=
ENST00000371953.8:c.1146C>G MANE Select	ENSP00000361021.3:p.Thr382=
ENST00000371953.7:c.1146C>G	ENSP00000361021.3:p.Thr382=
NM_000314.5:c.1146C>G	NP_000305.3:p.Thr382=
NM_000314.6:c.1146C>G	NP_000305.3:p.Thr382=
NM_001304717.2:c.1665C>G	NP_001291646.2:p.Thr555=
NM_001304718.1:c.555C>G	NP_001291647.1:p.Thr185=
XM_006717926.2:c.1101C>G	XP_006717989.1:p.Thr367=
XM_011539982.1:c.1050C>G	XP_011538284.1:p.Thr350=
XR_945791.1:n.1716C>G
NM_000314.7:c.1146C>G	NP_000305.3:p.Thr382=
NM_001304717.5:c.1665C>G	NP_001291646.4:p.Thr555=
NM_001304718.2:c.555C>G	NP_001291647.1:p.Thr185=
NM_000314.8:c.1146C>G MANE Select	NP_000305.3:p.Thr382=