Canonical Allele Identifier: CA2722434434

Gene: PTEN

Linked Data

• dbSNP Id: rs2132290518

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965488G>C , CM000672.2:g.87965488G>C	GRCh38
NC_000010.10:g.89725245G>C , CM000672.1:g.89725245G>C	GRCh37
NC_000010.9:g.89715225G>C	NCBI36
NG_007466.2:g.107050G>C , LRG_311:g.107050G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*16G>C	ENSP00000514759.2:n.*16G>C
ENST00000710265.1:c.*257G>C	ENSP00000518161.1:n.*257G>C
ENST00000688158.2:n.1963G>C
ENST00000688922.2:c.*1058G>C	ENSP00000508742.2:n.*1058G>C
ENST00000700021.1:c.*16G>C	ENSP00000514757.1:n.*16G>C
ENST00000700022.1:c.*567G>C	ENSP00000514758.1:n.*567G>C
ENST00000700023.1:n.2386G>C
ENST00000700024.1:n.2620G>C
ENST00000706954.1:c.*16G>C	ENSP00000516674.1:n.*16G>C
ENST00000706955.1:c.*1263G>C	ENSP00000516675.1:n.*1263G>C
ENST00000686459.1:c.*814G>C	ENSP00000508909.1:n.*814G>C
ENST00000688158.1:c.*1339G>C	ENSP00000509254.1:n.*1339G>C
ENST00000688308.1:c.*16G>C	ENSP00000508752.1:n.*16G>C
ENST00000688922.1:c.1149G>C
ENST00000693560.1:c.*16G>C	ENSP00000509861.1:n.*16G>C
ENST00000371953.8:c.*16G>C MANE Select	ENSP00000361021.3:n.*16G>C
ENST00000371953.7:c.*16G>C	ENSP00000361021.3:n.*16G>C
NM_000314.5:c.*16G>C	NP_000305.3:n.*16G>C
NM_000314.6:c.*16G>C	NP_000305.3:n.*16G>C
NM_001304717.2:c.*16G>C	NP_001291646.2:n.*16G>C
NM_001304718.1:c.*16G>C	NP_001291647.1:n.*16G>C
XM_006717926.2:c.*16G>C	XP_006717989.1:n.*16G>C
XM_011539982.1:c.*16G>C	XP_011538284.1:n.*16G>C
XR_945791.1:n.1798G>C
NM_000314.7:c.*16G>C	NP_000305.3:n.*16G>C
NM_001304717.5:c.*16G>C	NP_001291646.4:n.*16G>C
NM_001304718.2:c.*16G>C	NP_001291647.1:n.*16G>C
NM_000314.8:c.*16G>C MANE Select	NP_000305.3:n.*16G>C