Canonical Allele Identifier: CA377487352

Gene: PTEN

Linked Data

• dbSNP Id: rs2132290029
• MyVariant Identifiers: chr10:g.89725162C>T (hg19) ; chr10:g.87965405C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965405C>T , CM000672.2:g.87965405C>T	GRCh38
NC_000010.10:g.89725162C>T , CM000672.1:g.89725162C>T	GRCh37
NC_000010.9:g.89715142C>T	NCBI36
NG_007466.2:g.106967C>T , LRG_311:g.106967C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1238C>T	ENSP00000514759.2:p.Thr413Ile
ENST00000710265.1:c.*174C>T	ENSP00000518161.1:n.*174C>T
ENST00000688158.2:n.1880C>T
ENST00000688922.2:c.*975C>T	ENSP00000508742.2:n.*975C>T
ENST00000700021.1:c.1100C>T	ENSP00000514757.1:p.Thr367Ile
ENST00000700022.1:c.*484C>T	ENSP00000514758.1:n.*484C>T
ENST00000700023.1:n.2303C>T
ENST00000700024.1:n.2537C>T
ENST00000706954.1:c.1145C>T	ENSP00000516674.1:p.Thr382Ile
ENST00000706955.1:c.*1180C>T	ENSP00000516675.1:n.*1180C>T
ENST00000686459.1:c.*731C>T	ENSP00000508909.1:n.*731C>T
ENST00000688158.1:c.*1256C>T	ENSP00000509254.1:n.*1256C>T
ENST00000688308.1:c.1145C>T	ENSP00000508752.1:p.Thr382Ile
ENST00000688922.1:c.1066C>T
ENST00000693560.1:c.1664C>T	ENSP00000509861.1:p.Thr555Ile
ENST00000371953.8:c.1145C>T MANE Select	ENSP00000361021.3:p.Thr382Ile
ENST00000371953.7:c.1145C>T	ENSP00000361021.3:p.Thr382Ile
NM_000314.5:c.1145C>T	NP_000305.3:p.Thr382Ile
NM_000314.6:c.1145C>T	NP_000305.3:p.Thr382Ile
NM_001304717.2:c.1664C>T	NP_001291646.2:p.Thr555Ile
NM_001304718.1:c.554C>T	NP_001291647.1:p.Thr185Ile
XM_006717926.2:c.1100C>T	XP_006717989.1:p.Thr367Ile
XM_011539982.1:c.1049C>T	XP_011538284.1:p.Thr350Ile
XR_945791.1:n.1715C>T
NM_000314.7:c.1145C>T	NP_000305.3:p.Thr382Ile
NM_001304717.5:c.1664C>T	NP_001291646.4:p.Thr555Ile
NM_001304718.2:c.554C>T	NP_001291647.1:p.Thr185Ile
NM_000314.8:c.1145C>T MANE Select	NP_000305.3:p.Thr382Ile