Canonical Allele Identifier: CA2365869148
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651909C= , CM000682.2:g.44651909C= GRCh38
NC_000020.10:g.43280550C= , CM000682.1:g.43280550C= GRCh37
NC_000020.9:g.42713964C= NCBI36
NG_007385.1:g.4827G= , LRG_16:g.4827G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-128G= ENSP00000512234.1:n.-128G=
ENST00000696039.1:n.314G=
ENST00000696062.1:c.96+191G= ENSP00000512365.1:n.96+191G=
ENST00000696064.1:c.-125G= ENSP00000512367.1:n.-125G=
ENST00000696065.1:c.-128G= ENSP00000512368.1:n.-128G=
ENST00000535573.1:n.325G=
ENST00000536076.1:n.206G=
XM_011528479.1:c.-264G= XP_011526781.1:n.-264G=