Canonical Allele Identifier: CA2722434566

Gene: PTEN

Linked Data

• dbSNP Id: rs2132290557

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965497A>C , CM000672.2:g.87965497A>C	GRCh38
NC_000010.10:g.89725254A>C , CM000672.1:g.89725254A>C	GRCh37
NC_000010.9:g.89715234A>C	NCBI36
NG_007466.2:g.107059A>C , LRG_311:g.107059A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*25A>C	ENSP00000514759.2:n.*25A>C
ENST00000710265.1:c.*266A>C	ENSP00000518161.1:n.*266A>C
ENST00000688158.2:n.1972A>C
ENST00000688922.2:c.*1067A>C	ENSP00000508742.2:n.*1067A>C
ENST00000700021.1:c.*25A>C	ENSP00000514757.1:n.*25A>C
ENST00000700022.1:c.*576A>C	ENSP00000514758.1:n.*576A>C
ENST00000700023.1:n.2395A>C
ENST00000700024.1:n.2629A>C
ENST00000706954.1:c.*25A>C	ENSP00000516674.1:n.*25A>C
ENST00000706955.1:c.*1272A>C	ENSP00000516675.1:n.*1272A>C
ENST00000686459.1:c.*823A>C	ENSP00000508909.1:n.*823A>C
ENST00000688158.1:c.*1348A>C	ENSP00000509254.1:n.*1348A>C
ENST00000688308.1:c.*25A>C	ENSP00000508752.1:n.*25A>C
ENST00000688922.1:c.1158A>C
ENST00000693560.1:c.*25A>C	ENSP00000509861.1:n.*25A>C
ENST00000371953.8:c.*25A>C MANE Select	ENSP00000361021.3:n.*25A>C
ENST00000371953.7:c.*25A>C	ENSP00000361021.3:n.*25A>C
NM_000314.5:c.*25A>C	NP_000305.3:n.*25A>C
NM_000314.6:c.*25A>C	NP_000305.3:n.*25A>C
NM_001304717.2:c.*25A>C	NP_001291646.2:n.*25A>C
NM_001304718.1:c.*25A>C	NP_001291647.1:n.*25A>C
XM_006717926.2:c.*25A>C	XP_006717989.1:n.*25A>C
XM_011539982.1:c.*25A>C	XP_011538284.1:n.*25A>C
XR_945791.1:n.1807A>C
NM_000314.7:c.*25A>C	NP_000305.3:n.*25A>C
NM_001304717.5:c.*25A>C	NP_001291646.4:n.*25A>C
NM_001304718.2:c.*25A>C	NP_001291647.1:n.*25A>C
NM_000314.8:c.*25A>C MANE Select	NP_000305.3:n.*25A>C