Canonical Allele Identifier: CA2610045460

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863099T>G , CM000672.2:g.87863099T>G GRCh38
NC_000010.10:g.89622856T>G , CM000672.1:g.89622856T>G GRCh37
NC_000010.9:g.89612836T>G NCBI36
NG_007466.2:g.4662T>G , LRG_311:g.4662T>G
NG_033079.1:g.5339A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+457T>G (PTEN) ENSP00000516674.1:n.-17+457T>G
ENST00000688308.1:c.-31T>G (PTEN) ENSP00000508752.1:n.-31T>G
ENST00000445946.5:c.-612A>C (KLLN) MANE Select ENSP00000392204.2:n.-612A>C
ENST00000445946.3:c.-612A>C (KLLN) ENSP00000392204.2:n.-612A>C
NM_001126049.1:c.-612A>C (KLLN) NP_001119521.1:n.-612A>C
NM_001126049.2:c.-612A>C (KLLN) MANE Select NP_001119521.1:n.-612A>C