Canonical Allele Identifier: CA211259960

Gene: PTEN

Linked Data

• dbSNP Id: rs576331425
• gnomAD v3: 10-87966841-T-A
• gnomAD v4: 10-87966841-T-A
• MyVariant Identifiers: chr10:g.89726598T>A (hg19) ; chr10:g.87966841T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966841T>A , CM000672.2:g.87966841T>A	GRCh38
NC_000010.10:g.89726598T>A , CM000672.1:g.89726598T>A	GRCh37
NC_000010.9:g.89716578T>A	NCBI36
NG_007466.2:g.108403T>A , LRG_311:g.108403T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.*1369T>A	ENSP00000514759.2:n.*1369T>A
ENST00000710265.1:c.*1610T>A	ENSP00000518161.1:n.*1610T>A
ENST00000688158.2:n.3316T>A
ENST00000688922.2:c.*2411T>A	ENSP00000508742.2:n.*2411T>A
ENST00000700021.1:c.*1369T>A	ENSP00000514757.1:n.*1369T>A
ENST00000700024.1:n.3973T>A
ENST00000706954.1:c.*1369T>A	ENSP00000516674.1:n.*1369T>A
ENST00000706955.1:c.*2616T>A	ENSP00000516675.1:n.*2616T>A
ENST00000688158.1:c.*2692T>A	ENSP00000509254.1:n.*2692T>A
ENST00000688308.1:c.*1369T>A	ENSP00000508752.1:n.*1369T>A
ENST00000688922.1:c.2502T>A
ENST00000693560.1:c.*1369T>A	ENSP00000509861.1:n.*1369T>A
ENST00000371953.8:c.*1369T>A MANE Select	ENSP00000361021.3:n.*1369T>A
ENST00000371953.7:c.*1369T>A	ENSP00000361021.3:n.*1369T>A
NM_000314.5:c.*1369T>A	NP_000305.3:n.*1369T>A
NM_000314.6:c.*1369T>A	NP_000305.3:n.*1369T>A
NM_001304717.2:c.*1369T>A	NP_001291646.2:n.*1369T>A
NM_001304718.1:c.*1369T>A	NP_001291647.1:n.*1369T>A
XM_006717926.2:c.*1369T>A	XP_006717989.1:n.*1369T>A
XM_011539982.1:c.*1369T>A	XP_011538284.1:n.*1369T>A
XR_945791.1:n.3151T>A
NM_000314.7:c.*1369T>A	NP_000305.3:n.*1369T>A
NM_001304717.5:c.*1369T>A	NP_001291646.4:n.*1369T>A
NM_001304718.2:c.*1369T>A	NP_001291647.1:n.*1369T>A
NM_000314.8:c.*1369T>A MANE Select	NP_000305.3:n.*1369T>A