Canonical Allele Identifier: CA2365869166
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651931G= , CM000682.2:g.44651931G= GRCh38
NC_000020.10:g.43280572G= , CM000682.1:g.43280572G= GRCh37
NC_000020.9:g.42713986G= NCBI36
NG_007385.1:g.4805C= , LRG_16:g.4805C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-150C= ENSP00000512234.1:n.-150C=
ENST00000696039.1:n.292C=
ENST00000696062.1:c.96+169C= ENSP00000512365.1:n.96+169C=
ENST00000696064.1:c.-147C= ENSP00000512367.1:n.-147C=
ENST00000535573.1:n.303C=
ENST00000536076.1:n.184C=
XM_011528479.1:c.-286C= XP_011526781.1:n.-286C=