Canonical Allele Identifier: CA377486150

Gene: PTEN

Linked Data

• dbSNP Id: rs2132283655
• MyVariant Identifiers: chr10:g.89720862C>T (hg19) ; chr10:g.87961105C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961105C>T , CM000672.2:g.87961105C>T	GRCh38
NC_000010.10:g.89720862C>T , CM000672.1:g.89720862C>T	GRCh37
NC_000010.9:g.89710842C>T	NCBI36
NG_007466.2:g.102667C>T , LRG_311:g.102667C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1106C>T	ENSP00000514759.2:p.Ser369Phe
ENST00000710265.1:c.1013C>T	ENSP00000518161.1:p.Ser338Phe
ENST00000472832.3:c.1013C>T	ENSP00000483066.2:p.Ser338Phe
ENST00000688158.2:n.1748C>T
ENST00000688922.2:c.*843C>T	ENSP00000508742.2:n.*843C>T
ENST00000700021.1:c.968C>T	ENSP00000514757.1:p.Ser323Phe
ENST00000700022.1:c.*352C>T	ENSP00000514758.1:n.*352C>T
ENST00000700023.1:n.2171C>T
ENST00000700024.1:n.2405C>T
ENST00000700025.1:n.1782C>T
ENST00000700026.1:n.650C>T
ENST00000706954.1:c.1013C>T	ENSP00000516674.1:p.Ser338Phe
ENST00000706955.1:c.*1048C>T	ENSP00000516675.1:n.*1048C>T
ENST00000686459.1:c.*599C>T	ENSP00000508909.1:n.*599C>T
ENST00000688158.1:c.*1124C>T	ENSP00000509254.1:n.*1124C>T
ENST00000688308.1:c.1013C>T	ENSP00000508752.1:p.Ser338Phe
ENST00000688922.1:c.934C>T
ENST00000693560.1:c.1532C>T	ENSP00000509861.1:p.Ser511Phe
ENST00000371953.8:c.1013C>T MANE Select	ENSP00000361021.3:p.Ser338Phe
ENST00000371953.7:c.1013C>T	ENSP00000361021.3:p.Ser338Phe
ENST00000472832.2:c.440C>T	ENSP00000483066.1:p.Ser147Phe
NM_000314.5:c.1013C>T	NP_000305.3:p.Ser338Phe
NM_000314.6:c.1013C>T	NP_000305.3:p.Ser338Phe
NM_001304717.2:c.1532C>T	NP_001291646.2:p.Ser511Phe
NM_001304718.1:c.422C>T	NP_001291647.1:p.Ser141Phe
XM_006717926.2:c.968C>T	XP_006717989.1:p.Ser323Phe
XM_011539981.1:c.1013C>T	XP_011538283.1:p.Ser338Phe
XM_011539982.1:c.917C>T	XP_011538284.1:p.Ser306Phe
XR_945791.1:n.1583C>T
NM_000314.7:c.1013C>T	NP_000305.3:p.Ser338Phe
NM_001304717.5:c.1532C>T	NP_001291646.4:p.Ser511Phe
NM_001304718.2:c.422C>T	NP_001291647.1:p.Ser141Phe
NM_000314.8:c.1013C>T MANE Select	NP_000305.3:p.Ser338Phe