Canonical Allele Identifier: CA2610049842

Gene: PTEN

Linked Data

• gnomAD v4: 10-87967058-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967058G>T , CM000672.2:g.87967058G>T	GRCh38
NC_000010.10:g.89726815G>T , CM000672.1:g.89726815G>T	GRCh37
NC_000010.9:g.89716795G>T	NCBI36
NG_007466.2:g.108620G>T , LRG_311:g.108620G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1827G>T	ENSP00000518161.1:n.*1827G>T
ENST00000688158.2:n.3533G>T
ENST00000706954.1:c.*1586G>T	ENSP00000516674.1:n.*1586G>T
ENST00000706955.1:c.*2833G>T	ENSP00000516675.1:n.*2833G>T
ENST00000688158.1:c.*2909G>T	ENSP00000509254.1:n.*2909G>T
ENST00000693560.1:c.*1586G>T	ENSP00000509861.1:n.*1586G>T
ENST00000371953.8:c.*1586G>T MANE Select	ENSP00000361021.3:n.*1586G>T
ENST00000371953.7:c.*1586G>T	ENSP00000361021.3:n.*1586G>T
NM_000314.5:c.*1586G>T	NP_000305.3:n.*1586G>T
NM_000314.6:c.*1586G>T	NP_000305.3:n.*1586G>T
NM_001304717.2:c.*1586G>T	NP_001291646.2:n.*1586G>T
NM_001304718.1:c.*1586G>T	NP_001291647.1:n.*1586G>T
XM_006717926.2:c.*1586G>T	XP_006717989.1:n.*1586G>T
XM_011539982.1:c.*1586G>T	XP_011538284.1:n.*1586G>T
XR_945791.1:n.3368G>T
NM_000314.7:c.*1586G>T	NP_000305.3:n.*1586G>T
NM_001304717.5:c.*1586G>T	NP_001291646.4:n.*1586G>T
NM_001304718.2:c.*1586G>T	NP_001291647.1:n.*1586G>T
NM_000314.8:c.*1586G>T MANE Select	NP_000305.3:n.*1586G>T