Canonical Allele Identifier: CA2365869184
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651952T= , CM000682.2:g.44651952T= GRCh38
NC_000020.10:g.43280593T= , CM000682.1:g.43280593T= GRCh37
NC_000020.9:g.42714007T= NCBI36
NG_007385.1:g.4784A= , LRG_16:g.4784A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-171A= ENSP00000512234.1:n.-171A=
ENST00000696039.1:n.271A=
ENST00000696062.1:c.96+148A= ENSP00000512365.1:n.96+148A=
ENST00000696064.1:c.-168A= ENSP00000512367.1:n.-168A=
ENST00000535573.1:n.282A=
ENST00000536076.1:n.163A=
XM_011528479.1:c.-307A= XP_011526781.1:n.-307A=