Canonical Allele Identifier: CA377487368

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725170T>C (hg19) ; chr10:g.87965413T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965413T>C , CM000672.2:g.87965413T>C	GRCh38
NC_000010.10:g.89725170T>C , CM000672.1:g.89725170T>C	GRCh37
NC_000010.9:g.89715150T>C	NCBI36
NG_007466.2:g.106975T>C , LRG_311:g.106975T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1246T>C	ENSP00000514759.2:p.Ser416Pro
ENST00000710265.1:c.*182T>C	ENSP00000518161.1:n.*182T>C
ENST00000688158.2:n.1888T>C
ENST00000688922.2:c.*983T>C	ENSP00000508742.2:n.*983T>C
ENST00000700021.1:c.1108T>C	ENSP00000514757.1:p.Ser370Pro
ENST00000700022.1:c.*492T>C	ENSP00000514758.1:n.*492T>C
ENST00000700023.1:n.2311T>C
ENST00000700024.1:n.2545T>C
ENST00000706954.1:c.1153T>C	ENSP00000516674.1:p.Ser385Pro
ENST00000706955.1:c.*1188T>C	ENSP00000516675.1:n.*1188T>C
ENST00000686459.1:c.*739T>C	ENSP00000508909.1:n.*739T>C
ENST00000688158.1:c.*1264T>C	ENSP00000509254.1:n.*1264T>C
ENST00000688308.1:c.1153T>C	ENSP00000508752.1:p.Ser385Pro
ENST00000688922.1:c.1074T>C
ENST00000693560.1:c.1672T>C	ENSP00000509861.1:p.Ser558Pro
ENST00000371953.8:c.1153T>C MANE Select	ENSP00000361021.3:p.Ser385Pro
ENST00000371953.7:c.1153T>C	ENSP00000361021.3:p.Ser385Pro
NM_000314.5:c.1153T>C	NP_000305.3:p.Ser385Pro
NM_000314.6:c.1153T>C	NP_000305.3:p.Ser385Pro
NM_001304717.2:c.1672T>C	NP_001291646.2:p.Ser558Pro
NM_001304718.1:c.562T>C	NP_001291647.1:p.Ser188Pro
XM_006717926.2:c.1108T>C	XP_006717989.1:p.Ser370Pro
XM_011539982.1:c.1057T>C	XP_011538284.1:p.Ser353Pro
XR_945791.1:n.1723T>C
NM_000314.7:c.1153T>C	NP_000305.3:p.Ser385Pro
NM_001304717.5:c.1672T>C	NP_001291646.4:p.Ser558Pro
NM_001304718.2:c.562T>C	NP_001291647.1:p.Ser188Pro
NM_000314.8:c.1153T>C MANE Select	NP_000305.3:p.Ser385Pro