Canonical Allele Identifier: CA2610045724

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863181A>G , CM000672.2:g.87863181A>G GRCh38
NC_000010.10:g.89622938A>G , CM000672.1:g.89622938A>G GRCh37
NC_000010.9:g.89612918A>G NCBI36
NG_007466.2:g.4744A>G , LRG_311:g.4744A>G
NG_033079.1:g.5257T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+539A>G (PTEN) ENSP00000516674.1:n.-17+539A>G
ENST00000688308.1:c.-17+68A>G (PTEN) ENSP00000508752.1:n.-17+68A>G
ENST00000445946.5:c.-694T>C (KLLN) MANE Select ENSP00000392204.2:n.-694T>C
ENST00000371953.7:c.-1289A>G (PTEN) ENSP00000361021.3:n.-1289A>G
ENST00000445946.3:c.-694T>C (KLLN) ENSP00000392204.2:n.-694T>C
NM_001126049.1:c.-694T>C (KLLN) NP_001119521.1:n.-694T>C
NM_001126049.2:c.-694T>C (KLLN) MANE Select NP_001119521.1:n.-694T>C