Canonical Allele Identifier: CA2722336080

Gene: PTEN

Linked Data

• dbSNP Id: rs750772657

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957837G>C , CM000672.2:g.87957837G>C	GRCh38
NC_000010.10:g.89717594G>C , CM000672.1:g.89717594G>C	GRCh37
NC_000010.9:g.89707574G>C	NCBI36
NG_007466.2:g.99399G>C , LRG_311:g.99399G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.635-16G>C	ENSP00000514759.2:n.635-16G>C
ENST00000710265.1:c.635-16G>C	ENSP00000518161.1:n.635-16G>C
ENST00000472832.3:c.635-16G>C	ENSP00000483066.2:n.635-16G>C
ENST00000688158.2:n.1370-16G>C
ENST00000688922.2:c.*465-16G>C	ENSP00000508742.2:n.*465-16G>C
ENST00000700021.1:c.590-16G>C	ENSP00000514757.1:n.590-16G>C
ENST00000700022.1:c.493-16G>C	ENSP00000514758.1:n.493-16G>C
ENST00000700023.1:n.1793-16G>C
ENST00000700024.1:n.2027-16G>C
ENST00000700025.1:n.1404-16G>C
ENST00000700026.1:n.256G>C
ENST00000700029.1:c.469-16G>C
ENST00000706954.1:c.635-16G>C	ENSP00000516674.1:n.635-16G>C
ENST00000706955.1:c.*670-16G>C	ENSP00000516675.1:n.*670-16G>C
ENST00000686459.1:c.*221-16G>C	ENSP00000508909.1:n.*221-16G>C
ENST00000688158.1:c.*746-16G>C	ENSP00000509254.1:n.*746-16G>C
ENST00000688308.1:c.635-16G>C	ENSP00000508752.1:n.635-16G>C
ENST00000688922.1:c.556-16G>C
ENST00000693560.1:c.1154-16G>C	ENSP00000509861.1:n.1154-16G>C
ENST00000371953.8:c.635-16G>C MANE Select	ENSP00000361021.3:n.635-16G>C
ENST00000371953.7:c.635-16G>C	ENSP00000361021.3:n.635-16G>C
ENST00000472832.2:c.62-16G>C	ENSP00000483066.1:n.62-16G>C
NM_000314.5:c.635-16G>C	NP_000305.3:n.635-16G>C
NM_000314.6:c.635-16G>C	NP_000305.3:n.635-16G>C
NM_001304717.2:c.1154-16G>C	NP_001291646.2:n.1154-16G>C
NM_001304718.1:c.44-16G>C	NP_001291647.1:n.44-16G>C
XM_006717926.2:c.590-16G>C	XP_006717989.1:n.590-16G>C
XM_011539981.1:c.635-16G>C	XP_011538283.1:n.635-16G>C
XM_011539982.1:c.539-16G>C	XP_011538284.1:n.539-16G>C
XR_945791.1:n.1205-16G>C
NM_000314.7:c.635-16G>C	NP_000305.3:n.635-16G>C
NM_001304717.5:c.1154-16G>C	NP_001291646.4:n.1154-16G>C
NM_001304718.2:c.44-16G>C	NP_001291647.1:n.44-16G>C
NM_000314.8:c.635-16G>C MANE Select	NP_000305.3:n.635-16G>C