Canonical Allele Identifier: CA470671718

Gene: PTEN

Linked Data

• dbSNP Id: rs1064796017
• MyVariant Identifiers: chr10:g.89725223A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965466A>G , CM000672.2:g.87965466A>G	GRCh38
NC_000010.10:g.89725223A>G , CM000672.1:g.89725223A>G	GRCh37
NC_000010.9:g.89715203A>G	NCBI36
NG_007466.2:g.107028A>G , LRG_311:g.107028A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1299A>G	ENSP00000514759.2:p.Lys433=
ENST00000710265.1:c.*235A>G	ENSP00000518161.1:n.*235A>G
ENST00000688158.2:n.1941A>G
ENST00000688922.2:c.*1036A>G	ENSP00000508742.2:n.*1036A>G
ENST00000700021.1:c.1161A>G	ENSP00000514757.1:p.Lys387=
ENST00000700022.1:c.*545A>G	ENSP00000514758.1:n.*545A>G
ENST00000700023.1:n.2364A>G
ENST00000700024.1:n.2598A>G
ENST00000706954.1:c.1206A>G	ENSP00000516674.1:p.Lys402=
ENST00000706955.1:c.*1241A>G	ENSP00000516675.1:n.*1241A>G
ENST00000686459.1:c.*792A>G	ENSP00000508909.1:n.*792A>G
ENST00000688158.1:c.*1317A>G	ENSP00000509254.1:n.*1317A>G
ENST00000688308.1:c.1206A>G	ENSP00000508752.1:p.Lys402=
ENST00000688922.1:c.1127A>G
ENST00000693560.1:c.1725A>G	ENSP00000509861.1:p.Lys575=
ENST00000371953.8:c.1206A>G MANE Select	ENSP00000361021.3:p.Lys402=
ENST00000371953.7:c.1206A>G	ENSP00000361021.3:p.Lys402=
NM_000314.5:c.1206A>G	NP_000305.3:p.Lys402=
NM_000314.6:c.1206A>G	NP_000305.3:p.Lys402=
NM_001304717.2:c.1725A>G	NP_001291646.2:p.Lys575=
NM_001304718.1:c.615A>G	NP_001291647.1:p.Lys205=
XM_006717926.2:c.1161A>G	XP_006717989.1:p.Lys387=
XM_011539982.1:c.1110A>G	XP_011538284.1:p.Lys370=
XR_945791.1:n.1776A>G
NM_000314.7:c.1206A>G	NP_000305.3:p.Lys402=
NM_001304717.5:c.1725A>G	NP_001291646.4:p.Lys575=
NM_001304718.2:c.615A>G	NP_001291647.1:p.Lys205=
NM_000314.8:c.1206A>G MANE Select	NP_000305.3:p.Lys402=