Canonical Allele Identifier: CA377487212

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725100T>G (hg19) ; chr10:g.87965343T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965343T>G , CM000672.2:g.87965343T>G	GRCh38
NC_000010.10:g.89725100T>G , CM000672.1:g.89725100T>G	GRCh37
NC_000010.9:g.89715080T>G	NCBI36
NG_007466.2:g.106905T>G , LRG_311:g.106905T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1176T>G	ENSP00000514759.2:p.Ser392Arg
ENST00000710265.1:c.*112T>G	ENSP00000518161.1:n.*112T>G
ENST00000688158.2:n.1818T>G
ENST00000688922.2:c.*913T>G	ENSP00000508742.2:n.*913T>G
ENST00000700021.1:c.1038T>G	ENSP00000514757.1:p.Ser346Arg
ENST00000700022.1:c.*422T>G	ENSP00000514758.1:n.*422T>G
ENST00000700023.1:n.2241T>G
ENST00000700024.1:n.2475T>G
ENST00000706954.1:c.1083T>G	ENSP00000516674.1:p.Ser361Arg
ENST00000706955.1:c.*1118T>G	ENSP00000516675.1:n.*1118T>G
ENST00000686459.1:c.*669T>G	ENSP00000508909.1:n.*669T>G
ENST00000688158.1:c.*1194T>G	ENSP00000509254.1:n.*1194T>G
ENST00000688308.1:c.1083T>G	ENSP00000508752.1:p.Ser361Arg
ENST00000688922.1:c.1004T>G
ENST00000693560.1:c.1602T>G	ENSP00000509861.1:p.Ser534Arg
ENST00000371953.8:c.1083T>G MANE Select	ENSP00000361021.3:p.Ser361Arg
ENST00000371953.7:c.1083T>G	ENSP00000361021.3:p.Ser361Arg
NM_000314.5:c.1083T>G	NP_000305.3:p.Ser361Arg
NM_000314.6:c.1083T>G	NP_000305.3:p.Ser361Arg
NM_001304717.2:c.1602T>G	NP_001291646.2:p.Ser534Arg
NM_001304718.1:c.492T>G	NP_001291647.1:p.Ser164Arg
XM_006717926.2:c.1038T>G	XP_006717989.1:p.Ser346Arg
XM_011539982.1:c.987T>G	XP_011538284.1:p.Ser329Arg
XR_945791.1:n.1653T>G
NM_000314.7:c.1083T>G	NP_000305.3:p.Ser361Arg
NM_001304717.5:c.1602T>G	NP_001291646.4:p.Ser534Arg
NM_001304718.2:c.492T>G	NP_001291647.1:p.Ser164Arg
NM_000314.8:c.1083T>G MANE Select	NP_000305.3:p.Ser361Arg