Canonical Allele Identifier: CA211260686

Gene: PTEN

Linked Data

• dbSNP Id: rs937529889
• gnomAD v3: 10-87967507-C-T
• gnomAD v4: 10-87967507-C-T
• MyVariant Identifiers: chr10:g.87967507C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967507C>T , CM000672.2:g.87967507C>T	GRCh38
NC_000010.10:g.89727264C>T , CM000672.1:g.89727264C>T	GRCh37
NC_000010.9:g.89717244C>T	NCBI36
NG_007466.2:g.109069C>T , LRG_311:g.109069C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2276C>T	ENSP00000518161.1:n.*2276C>T
ENST00000688158.2:n.3982C>T
ENST00000706954.1:c.*2035C>T	ENSP00000516674.1:n.*2035C>T
ENST00000706955.1:c.*3282C>T	ENSP00000516675.1:n.*3282C>T
ENST00000688158.1:c.*3358C>T	ENSP00000509254.1:n.*3358C>T
ENST00000693560.1:c.*2035C>T	ENSP00000509861.1:n.*2035C>T
ENST00000371953.8:c.*2035C>T MANE Select	ENSP00000361021.3:n.*2035C>T
ENST00000371953.7:c.*2035C>T	ENSP00000361021.3:n.*2035C>T
NM_000314.5:c.*2035C>T	NP_000305.3:n.*2035C>T
NM_000314.6:c.*2035C>T	NP_000305.3:n.*2035C>T
NM_001304717.2:c.*2035C>T	NP_001291646.2:n.*2035C>T
NM_001304718.1:c.*2035C>T	NP_001291647.1:n.*2035C>T
XM_006717926.2:c.*2035C>T	XP_006717989.1:n.*2035C>T
XM_011539982.1:c.*2035C>T	XP_011538284.1:n.*2035C>T
XR_945791.1:n.3817C>T
NM_000314.7:c.*2035C>T	NP_000305.3:n.*2035C>T
NM_001304717.5:c.*2035C>T	NP_001291646.4:n.*2035C>T
NM_001304718.2:c.*2035C>T	NP_001291647.1:n.*2035C>T
NM_000314.8:c.*2035C>T MANE Select	NP_000305.3:n.*2035C>T