Canonical Allele Identifier: CA470670026
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1860551372
MyVariant Identifiers: chr10:g.89717764G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958007G>A , CM000672.2:g.87958007G>A GRCh38
NC_000010.10:g.89717764G>A , CM000672.1:g.89717764G>A GRCh37
NC_000010.9:g.89707744G>A NCBI36
NG_007466.2:g.99569G>A , LRG_311:g.99569G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.789G>A ENSP00000514759.2:p.Lys263=
ENST00000710265.1:c.789G>A ENSP00000518161.1:p.Lys263=
ENST00000472832.3:c.789G>A ENSP00000483066.2:p.Lys263=
ENST00000688158.2:n.1524G>A
ENST00000688922.2:c.*619G>A ENSP00000508742.2:n.*619G>A
ENST00000700021.1:c.744G>A ENSP00000514757.1:p.Lys248=
ENST00000700022.1:c.*128G>A ENSP00000514758.1:n.*128G>A
ENST00000700023.1:n.1947G>A
ENST00000700024.1:n.2181G>A
ENST00000700025.1:n.1558G>A
ENST00000700026.1:n.426G>A
ENST00000700029.1:c.623G>A
ENST00000706954.1:c.789G>A ENSP00000516674.1:p.Lys263=
ENST00000706955.1:c.*824G>A ENSP00000516675.1:n.*824G>A
ENST00000686459.1:c.*375G>A ENSP00000508909.1:n.*375G>A
ENST00000688158.1:c.*900G>A ENSP00000509254.1:n.*900G>A
ENST00000688308.1:c.789G>A ENSP00000508752.1:p.Lys263=
ENST00000688922.1:c.710G>A
ENST00000693560.1:c.1308G>A ENSP00000509861.1:p.Lys436=
ENST00000371953.8:c.789G>A MANE Select ENSP00000361021.3:p.Lys263=
ENST00000371953.7:c.789G>A ENSP00000361021.3:p.Lys263=
ENST00000472832.2:c.216G>A ENSP00000483066.1:p.Lys72=
NM_000314.5:c.789G>A NP_000305.3:p.Lys263=
NM_000314.6:c.789G>A NP_000305.3:p.Lys263=
NM_001304717.2:c.1308G>A NP_001291646.2:p.Lys436=
NM_001304718.1:c.198G>A NP_001291647.1:p.Lys66=
XM_006717926.2:c.744G>A XP_006717989.1:p.Lys248=
XM_011539981.1:c.789G>A XP_011538283.1:p.Lys263=
XM_011539982.1:c.693G>A XP_011538284.1:p.Lys231=
XR_945791.1:n.1359G>A
NM_000314.7:c.789G>A NP_000305.3:p.Lys263=
NM_001304717.5:c.1308G>A NP_001291646.4:p.Lys436=
NM_001304718.2:c.198G>A NP_001291647.1:p.Lys66=
NM_000314.8:c.789G>A MANE Select NP_000305.3:p.Lys263=