Canonical Allele Identifier: CA2365869188
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651962A= , CM000682.2:g.44651962A= GRCh38
NC_000020.10:g.43280603A= , CM000682.1:g.43280603A= GRCh37
NC_000020.9:g.42714017A= NCBI36
NG_007385.1:g.4774T= , LRG_16:g.4774T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-181T= ENSP00000512234.1:n.-181T=
ENST00000696039.1:n.261T=
ENST00000696062.1:c.96+138T= ENSP00000512365.1:n.96+138T=
ENST00000696064.1:c.-178T= ENSP00000512367.1:n.-178T=
ENST00000535573.1:n.272T=
ENST00000536076.1:n.153T=
XM_011528479.1:c.-317T= XP_011526781.1:n.-317T=