Canonical Allele Identifier: CA377487185

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725087C>A (hg19) ; chr10:g.87965330C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965330C>A , CM000672.2:g.87965330C>A	GRCh38
NC_000010.10:g.89725087C>A , CM000672.1:g.89725087C>A	GRCh37
NC_000010.9:g.89715067C>A	NCBI36
NG_007466.2:g.106892C>A , LRG_311:g.106892C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1163C>A	ENSP00000514759.2:p.Pro388Gln
ENST00000710265.1:c.*99C>A	ENSP00000518161.1:n.*99C>A
ENST00000688158.2:n.1805C>A
ENST00000688922.2:c.*900C>A	ENSP00000508742.2:n.*900C>A
ENST00000700021.1:c.1025C>A	ENSP00000514757.1:p.Pro342Gln
ENST00000700022.1:c.*409C>A	ENSP00000514758.1:n.*409C>A
ENST00000700023.1:n.2228C>A
ENST00000700024.1:n.2462C>A
ENST00000706954.1:c.1070C>A	ENSP00000516674.1:p.Pro357Gln
ENST00000706955.1:c.*1105C>A	ENSP00000516675.1:n.*1105C>A
ENST00000686459.1:c.*656C>A	ENSP00000508909.1:n.*656C>A
ENST00000688158.1:c.*1181C>A	ENSP00000509254.1:n.*1181C>A
ENST00000688308.1:c.1070C>A	ENSP00000508752.1:p.Pro357Gln
ENST00000688922.1:c.991C>A
ENST00000693560.1:c.1589C>A	ENSP00000509861.1:p.Pro530Gln
ENST00000371953.8:c.1070C>A MANE Select	ENSP00000361021.3:p.Pro357Gln
ENST00000371953.7:c.1070C>A	ENSP00000361021.3:p.Pro357Gln
NM_000314.5:c.1070C>A	NP_000305.3:p.Pro357Gln
NM_000314.6:c.1070C>A	NP_000305.3:p.Pro357Gln
NM_001304717.2:c.1589C>A	NP_001291646.2:p.Pro530Gln
NM_001304718.1:c.479C>A	NP_001291647.1:p.Pro160Gln
XM_006717926.2:c.1025C>A	XP_006717989.1:p.Pro342Gln
XM_011539982.1:c.974C>A	XP_011538284.1:p.Pro325Gln
XR_945791.1:n.1640C>A
NM_000314.7:c.1070C>A	NP_000305.3:p.Pro357Gln
NM_001304717.5:c.1589C>A	NP_001291646.4:p.Pro530Gln
NM_001304718.2:c.479C>A	NP_001291647.1:p.Pro160Gln
NM_000314.8:c.1070C>A MANE Select	NP_000305.3:p.Pro357Gln