Canonical Allele Identifier: CA377487172

Gene: PTEN

Linked Data

• dbSNP Id: rs2132289414
• MyVariant Identifiers: chr10:g.89725080T>C (hg19) ; chr10:g.87965323T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965323T>C , CM000672.2:g.87965323T>C	GRCh38
NC_000010.10:g.89725080T>C , CM000672.1:g.89725080T>C	GRCh37
NC_000010.9:g.89715060T>C	NCBI36
NG_007466.2:g.106885T>C , LRG_311:g.106885T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1156T>C	ENSP00000514759.2:p.Ser386Pro
ENST00000710265.1:c.*92T>C	ENSP00000518161.1:n.*92T>C
ENST00000688158.2:n.1798T>C
ENST00000688922.2:c.*893T>C	ENSP00000508742.2:n.*893T>C
ENST00000700021.1:c.1018T>C	ENSP00000514757.1:p.Ser340Pro
ENST00000700022.1:c.*402T>C	ENSP00000514758.1:n.*402T>C
ENST00000700023.1:n.2221T>C
ENST00000700024.1:n.2455T>C
ENST00000706954.1:c.1063T>C	ENSP00000516674.1:p.Ser355Pro
ENST00000706955.1:c.*1098T>C	ENSP00000516675.1:n.*1098T>C
ENST00000686459.1:c.*649T>C	ENSP00000508909.1:n.*649T>C
ENST00000688158.1:c.*1174T>C	ENSP00000509254.1:n.*1174T>C
ENST00000688308.1:c.1063T>C	ENSP00000508752.1:p.Ser355Pro
ENST00000688922.1:c.984T>C
ENST00000693560.1:c.1582T>C	ENSP00000509861.1:p.Ser528Pro
ENST00000371953.8:c.1063T>C MANE Select	ENSP00000361021.3:p.Ser355Pro
ENST00000371953.7:c.1063T>C	ENSP00000361021.3:p.Ser355Pro
NM_000314.5:c.1063T>C	NP_000305.3:p.Ser355Pro
NM_000314.6:c.1063T>C	NP_000305.3:p.Ser355Pro
NM_001304717.2:c.1582T>C	NP_001291646.2:p.Ser528Pro
NM_001304718.1:c.472T>C	NP_001291647.1:p.Ser158Pro
XM_006717926.2:c.1018T>C	XP_006717989.1:p.Ser340Pro
XM_011539982.1:c.967T>C	XP_011538284.1:p.Ser323Pro
XR_945791.1:n.1633T>C
NM_000314.7:c.1063T>C	NP_000305.3:p.Ser355Pro
NM_001304717.5:c.1582T>C	NP_001291646.4:p.Ser528Pro
NM_001304718.2:c.472T>C	NP_001291647.1:p.Ser158Pro
NM_000314.8:c.1063T>C MANE Select	NP_000305.3:p.Ser355Pro