Canonical Allele Identifier: CA2365869156
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651917C= , CM000682.2:g.44651917C= GRCh38
NC_000020.10:g.43280558C= , CM000682.1:g.43280558C= GRCh37
NC_000020.9:g.42713972C= NCBI36
NG_007385.1:g.4819G= , LRG_16:g.4819G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-136G= ENSP00000512234.1:n.-136G=
ENST00000696039.1:n.306G=
ENST00000696062.1:c.96+183G= ENSP00000512365.1:n.96+183G=
ENST00000696064.1:c.-133G= ENSP00000512367.1:n.-133G=
ENST00000535573.1:n.317G=
ENST00000536076.1:n.198G=
XM_011528479.1:c.-272G= XP_011526781.1:n.-272G=