Canonical Allele Identifier: CA2610046152

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863436G>C , CM000672.2:g.87863436G>C GRCh38
NC_000010.10:g.89623193G>C , CM000672.1:g.89623193G>C GRCh37
NC_000010.9:g.89613173G>C NCBI36
NG_007466.2:g.4999G>C , LRG_311:g.4999G>C
NG_033079.1:g.5002C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+794G>C (PTEN) ENSP00000516674.1:n.-17+794G>C
ENST00000688308.1:c.-17+323G>C (PTEN) ENSP00000508752.1:n.-17+323G>C
ENST00000445946.5:c.-949C>G (KLLN) MANE Select ENSP00000392204.2:n.-949C>G
ENST00000371953.7:c.-1034G>C (PTEN) ENSP00000361021.3:n.-1034G>C
ENST00000445946.3:c.-949C>G (KLLN) ENSP00000392204.2:n.-949C>G
NM_001126049.1:c.-949C>G (KLLN) NP_001119521.1:n.-949C>G
NM_001126049.2:c.-949C>G (KLLN) MANE Select NP_001119521.1:n.-949C>G