Canonical Allele Identifier: CA2610049826

Gene: PTEN

Linked Data

• gnomAD v4: 10-87966987-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966987C>A , CM000672.2:g.87966987C>A	GRCh38
NC_000010.10:g.89726744C>A , CM000672.1:g.89726744C>A	GRCh37
NC_000010.9:g.89716724C>A	NCBI36
NG_007466.2:g.108549C>A , LRG_311:g.108549C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1756C>A	ENSP00000518161.1:n.*1756C>A
ENST00000688158.2:n.3462C>A
ENST00000706954.1:c.*1515C>A	ENSP00000516674.1:n.*1515C>A
ENST00000706955.1:c.*2762C>A	ENSP00000516675.1:n.*2762C>A
ENST00000688158.1:c.*2838C>A	ENSP00000509254.1:n.*2838C>A
ENST00000693560.1:c.*1515C>A	ENSP00000509861.1:n.*1515C>A
ENST00000371953.8:c.*1515C>A MANE Select	ENSP00000361021.3:n.*1515C>A
ENST00000371953.7:c.*1515C>A	ENSP00000361021.3:n.*1515C>A
NM_000314.5:c.*1515C>A	NP_000305.3:n.*1515C>A
NM_000314.6:c.*1515C>A	NP_000305.3:n.*1515C>A
NM_001304717.2:c.*1515C>A	NP_001291646.2:n.*1515C>A
NM_001304718.1:c.*1515C>A	NP_001291647.1:n.*1515C>A
XM_006717926.2:c.*1515C>A	XP_006717989.1:n.*1515C>A
XM_011539982.1:c.*1515C>A	XP_011538284.1:n.*1515C>A
XR_945791.1:n.3297C>A
NM_000314.7:c.*1515C>A	NP_000305.3:n.*1515C>A
NM_001304717.5:c.*1515C>A	NP_001291646.4:n.*1515C>A
NM_001304718.2:c.*1515C>A	NP_001291647.1:n.*1515C>A
NM_000314.8:c.*1515C>A MANE Select	NP_000305.3:n.*1515C>A