Canonical Allele Identifier: CA377487262

Gene: PTEN

Linked Data

• dbSNP Id: rs2132289741
• MyVariant Identifiers: chr10:g.89725126G>C (hg19) ; chr10:g.87965369G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965369G>C , CM000672.2:g.87965369G>C	GRCh38
NC_000010.10:g.89725126G>C , CM000672.1:g.89725126G>C	GRCh37
NC_000010.9:g.89715106G>C	NCBI36
NG_007466.2:g.106931G>C , LRG_311:g.106931G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1202G>C	ENSP00000514759.2:p.Ser401Thr
ENST00000710265.1:c.*138G>C	ENSP00000518161.1:n.*138G>C
ENST00000688158.2:n.1844G>C
ENST00000688922.2:c.*939G>C	ENSP00000508742.2:n.*939G>C
ENST00000700021.1:c.1064G>C	ENSP00000514757.1:p.Ser355Thr
ENST00000700022.1:c.*448G>C	ENSP00000514758.1:n.*448G>C
ENST00000700023.1:n.2267G>C
ENST00000700024.1:n.2501G>C
ENST00000706954.1:c.1109G>C	ENSP00000516674.1:p.Ser370Thr
ENST00000706955.1:c.*1144G>C	ENSP00000516675.1:n.*1144G>C
ENST00000686459.1:c.*695G>C	ENSP00000508909.1:n.*695G>C
ENST00000688158.1:c.*1220G>C	ENSP00000509254.1:n.*1220G>C
ENST00000688308.1:c.1109G>C	ENSP00000508752.1:p.Ser370Thr
ENST00000688922.1:c.1030G>C
ENST00000693560.1:c.1628G>C	ENSP00000509861.1:p.Ser543Thr
ENST00000371953.8:c.1109G>C MANE Select	ENSP00000361021.3:p.Ser370Thr
ENST00000371953.7:c.1109G>C	ENSP00000361021.3:p.Ser370Thr
NM_000314.5:c.1109G>C	NP_000305.3:p.Ser370Thr
NM_000314.6:c.1109G>C	NP_000305.3:p.Ser370Thr
NM_001304717.2:c.1628G>C	NP_001291646.2:p.Ser543Thr
NM_001304718.1:c.518G>C	NP_001291647.1:p.Ser173Thr
XM_006717926.2:c.1064G>C	XP_006717989.1:p.Ser355Thr
XM_011539982.1:c.1013G>C	XP_011538284.1:p.Ser338Thr
XR_945791.1:n.1679G>C
NM_000314.7:c.1109G>C	NP_000305.3:p.Ser370Thr
NM_001304717.5:c.1628G>C	NP_001291646.4:p.Ser543Thr
NM_001304718.2:c.518G>C	NP_001291647.1:p.Ser173Thr
NM_000314.8:c.1109G>C MANE Select	NP_000305.3:p.Ser370Thr