Canonical Allele Identifier: CA2610045649

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863156T>C , CM000672.2:g.87863156T>C GRCh38
NC_000010.10:g.89622913T>C , CM000672.1:g.89622913T>C GRCh37
NC_000010.9:g.89612893T>C NCBI36
NG_007466.2:g.4719T>C , LRG_311:g.4719T>C
NG_033079.1:g.5282A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+514T>C (PTEN) ENSP00000516674.1:n.-17+514T>C
ENST00000688308.1:c.-17+43T>C (PTEN) ENSP00000508752.1:n.-17+43T>C
ENST00000445946.5:c.-669A>G (KLLN) MANE Select ENSP00000392204.2:n.-669A>G
ENST00000371953.7:c.-1314T>C (PTEN) ENSP00000361021.3:n.-1314T>C
ENST00000445946.3:c.-669A>G (KLLN) ENSP00000392204.2:n.-669A>G
NM_001126049.1:c.-669A>G (KLLN) NP_001119521.1:n.-669A>G
NM_001126049.2:c.-669A>G (KLLN) MANE Select NP_001119521.1:n.-669A>G