Canonical Allele Identifier: CA377487492

Gene: PTEN

Linked Data

• dbSNP Id: rs2132290401
• MyVariant Identifiers: chr10:g.89725222A>T (hg19) ; chr10:g.87965465A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965465A>T , CM000672.2:g.87965465A>T	GRCh38
NC_000010.10:g.89725222A>T , CM000672.1:g.89725222A>T	GRCh37
NC_000010.9:g.89715202A>T	NCBI36
NG_007466.2:g.107027A>T , LRG_311:g.107027A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1298A>T	ENSP00000514759.2:p.Lys433Ile
ENST00000710265.1:c.*234A>T	ENSP00000518161.1:n.*234A>T
ENST00000688158.2:n.1940A>T
ENST00000688922.2:c.*1035A>T	ENSP00000508742.2:n.*1035A>T
ENST00000700021.1:c.1160A>T	ENSP00000514757.1:p.Lys387Ile
ENST00000700022.1:c.*544A>T	ENSP00000514758.1:n.*544A>T
ENST00000700023.1:n.2363A>T
ENST00000700024.1:n.2597A>T
ENST00000706954.1:c.1205A>T	ENSP00000516674.1:p.Lys402Ile
ENST00000706955.1:c.*1240A>T	ENSP00000516675.1:n.*1240A>T
ENST00000686459.1:c.*791A>T	ENSP00000508909.1:n.*791A>T
ENST00000688158.1:c.*1316A>T	ENSP00000509254.1:n.*1316A>T
ENST00000688308.1:c.1205A>T	ENSP00000508752.1:p.Lys402Ile
ENST00000688922.1:c.1126A>T
ENST00000693560.1:c.1724A>T	ENSP00000509861.1:p.Lys575Ile
ENST00000371953.8:c.1205A>T MANE Select	ENSP00000361021.3:p.Lys402Ile
ENST00000371953.7:c.1205A>T	ENSP00000361021.3:p.Lys402Ile
NM_000314.5:c.1205A>T	NP_000305.3:p.Lys402Ile
NM_000314.6:c.1205A>T	NP_000305.3:p.Lys402Ile
NM_001304717.2:c.1724A>T	NP_001291646.2:p.Lys575Ile
NM_001304718.1:c.614A>T	NP_001291647.1:p.Lys205Ile
XM_006717926.2:c.1160A>T	XP_006717989.1:p.Lys387Ile
XM_011539982.1:c.1109A>T	XP_011538284.1:p.Lys370Ile
XR_945791.1:n.1775A>T
NM_000314.7:c.1205A>T	NP_000305.3:p.Lys402Ile
NM_001304717.5:c.1724A>T	NP_001291646.4:p.Lys575Ile
NM_001304718.2:c.614A>T	NP_001291647.1:p.Lys205Ile
NM_000314.8:c.1205A>T MANE Select	NP_000305.3:p.Lys402Ile