Canonical Allele Identifier: CA2610049774

Gene: PTEN

Linked Data

• gnomAD v4: 10-87966713-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966713C>A , CM000672.2:g.87966713C>A	GRCh38
NC_000010.10:g.89726470C>A , CM000672.1:g.89726470C>A	GRCh37
NC_000010.9:g.89716450C>A	NCBI36
NG_007466.2:g.108275C>A , LRG_311:g.108275C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*1241C>A	ENSP00000514759.2:n.*1241C>A
ENST00000710265.1:c.*1482C>A	ENSP00000518161.1:n.*1482C>A
ENST00000688158.2:n.3188C>A
ENST00000688922.2:c.*2283C>A	ENSP00000508742.2:n.*2283C>A
ENST00000700021.1:c.*1241C>A	ENSP00000514757.1:n.*1241C>A
ENST00000700022.1:c.*1792C>A	ENSP00000514758.1:n.*1792C>A
ENST00000700024.1:n.3845C>A
ENST00000706954.1:c.*1241C>A	ENSP00000516674.1:n.*1241C>A
ENST00000706955.1:c.*2488C>A	ENSP00000516675.1:n.*2488C>A
ENST00000688158.1:c.*2564C>A	ENSP00000509254.1:n.*2564C>A
ENST00000688308.1:c.*1241C>A	ENSP00000508752.1:n.*1241C>A
ENST00000688922.1:c.2374C>A
ENST00000693560.1:c.*1241C>A	ENSP00000509861.1:n.*1241C>A
ENST00000371953.8:c.*1241C>A MANE Select	ENSP00000361021.3:n.*1241C>A
ENST00000371953.7:c.*1241C>A	ENSP00000361021.3:n.*1241C>A
NM_000314.5:c.*1241C>A	NP_000305.3:n.*1241C>A
NM_000314.6:c.*1241C>A	NP_000305.3:n.*1241C>A
NM_001304717.2:c.*1241C>A	NP_001291646.2:n.*1241C>A
NM_001304718.1:c.*1241C>A	NP_001291647.1:n.*1241C>A
XM_006717926.2:c.*1241C>A	XP_006717989.1:n.*1241C>A
XM_011539982.1:c.*1241C>A	XP_011538284.1:n.*1241C>A
XR_945791.1:n.3023C>A
NM_000314.7:c.*1241C>A	NP_000305.3:n.*1241C>A
NM_001304717.5:c.*1241C>A	NP_001291646.4:n.*1241C>A
NM_001304718.2:c.*1241C>A	NP_001291647.1:n.*1241C>A
NM_000314.8:c.*1241C>A MANE Select	NP_000305.3:n.*1241C>A