Canonical Allele Identifier: CA2816478429
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651949G>C , CM000682.2:g.44651949G>C GRCh38
NC_000020.10:g.43280590G>C , CM000682.1:g.43280590G>C GRCh37
NC_000020.9:g.42714004G>C NCBI36
NG_007385.1:g.4787C>G , LRG_16:g.4787C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-168C>G ENSP00000512234.1:n.-168C>G
ENST00000696039.1:n.274C>G
ENST00000696062.1:c.96+151C>G ENSP00000512365.1:n.96+151C>G
ENST00000696064.1:c.-165C>G ENSP00000512367.1:n.-165C>G
ENST00000535573.1:n.285C>G
ENST00000536076.1:n.166C>G
XM_011528479.1:c.-304C>G XP_011526781.1:n.-304C>G