Canonical Allele Identifier: CA2365869152
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651912G= , CM000682.2:g.44651912G= GRCh38
NC_000020.10:g.43280553G= , CM000682.1:g.43280553G= GRCh37
NC_000020.9:g.42713967G= NCBI36
NG_007385.1:g.4824C= , LRG_16:g.4824C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-131C= ENSP00000512234.1:n.-131C=
ENST00000696039.1:n.311C=
ENST00000696062.1:c.96+188C= ENSP00000512365.1:n.96+188C=
ENST00000696064.1:c.-128C= ENSP00000512367.1:n.-128C=
ENST00000696065.1:c.-131C= ENSP00000512368.1:n.-131C=
ENST00000535573.1:n.322C=
ENST00000536076.1:n.203C=
XM_011528479.1:c.-267C= XP_011526781.1:n.-267C=