Canonical Allele Identifier: CA377487165

Gene: PTEN

Linked Data

• dbSNP Id: rs772784762
• MyVariant Identifiers: chr10:g.89725076G>C (hg19) ; chr10:g.87965319G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965319G>C , CM000672.2:g.87965319G>C	GRCh38
NC_000010.10:g.89725076G>C , CM000672.1:g.89725076G>C	GRCh37
NC_000010.9:g.89715056G>C	NCBI36
NG_007466.2:g.106881G>C , LRG_311:g.106881G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1152G>C	ENSP00000514759.2:p.Glu384Asp
ENST00000710265.1:c.*88G>C	ENSP00000518161.1:n.*88G>C
ENST00000688158.2:n.1794G>C
ENST00000688922.2:c.*889G>C	ENSP00000508742.2:n.*889G>C
ENST00000700021.1:c.1014G>C	ENSP00000514757.1:p.Glu338Asp
ENST00000700022.1:c.*398G>C	ENSP00000514758.1:n.*398G>C
ENST00000700023.1:n.2217G>C
ENST00000700024.1:n.2451G>C
ENST00000706954.1:c.1059G>C	ENSP00000516674.1:p.Glu353Asp
ENST00000706955.1:c.*1094G>C	ENSP00000516675.1:n.*1094G>C
ENST00000686459.1:c.*645G>C	ENSP00000508909.1:n.*645G>C
ENST00000688158.1:c.*1170G>C	ENSP00000509254.1:n.*1170G>C
ENST00000688308.1:c.1059G>C	ENSP00000508752.1:p.Glu353Asp
ENST00000688922.1:c.980G>C
ENST00000693560.1:c.1578G>C	ENSP00000509861.1:p.Glu526Asp
ENST00000371953.8:c.1059G>C MANE Select	ENSP00000361021.3:p.Glu353Asp
ENST00000371953.7:c.1059G>C	ENSP00000361021.3:p.Glu353Asp
NM_000314.5:c.1059G>C	NP_000305.3:p.Glu353Asp
NM_000314.6:c.1059G>C	NP_000305.3:p.Glu353Asp
NM_001304717.2:c.1578G>C	NP_001291646.2:p.Glu526Asp
NM_001304718.1:c.468G>C	NP_001291647.1:p.Glu156Asp
XM_006717926.2:c.1014G>C	XP_006717989.1:p.Glu338Asp
XM_011539982.1:c.963G>C	XP_011538284.1:p.Glu321Asp
XR_945791.1:n.1629G>C
NM_000314.7:c.1059G>C	NP_000305.3:p.Glu353Asp
NM_001304717.5:c.1578G>C	NP_001291646.4:p.Glu526Asp
NM_001304718.2:c.468G>C	NP_001291647.1:p.Glu156Asp
NM_000314.8:c.1059G>C MANE Select	NP_000305.3:p.Glu353Asp