Canonical Allele Identifier: CA2365869162
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651926T= , CM000682.2:g.44651926T= GRCh38
NC_000020.10:g.43280567T= , CM000682.1:g.43280567T= GRCh37
NC_000020.9:g.42713981T= NCBI36
NG_007385.1:g.4810A= , LRG_16:g.4810A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-145A= ENSP00000512234.1:n.-145A=
ENST00000696039.1:n.297A=
ENST00000696062.1:c.96+174A= ENSP00000512365.1:n.96+174A=
ENST00000696064.1:c.-142A= ENSP00000512367.1:n.-142A=
ENST00000535573.1:n.308A=
ENST00000536076.1:n.189A=
XM_011528479.1:c.-281A= XP_011526781.1:n.-281A=