Canonical Allele Identifier: CA2365869170
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651937T= , CM000682.2:g.44651937T= GRCh38
NC_000020.10:g.43280578T= , CM000682.1:g.43280578T= GRCh37
NC_000020.9:g.42713992T= NCBI36
NG_007385.1:g.4799A= , LRG_16:g.4799A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-156A= ENSP00000512234.1:n.-156A=
ENST00000696039.1:n.286A=
ENST00000696062.1:c.96+163A= ENSP00000512365.1:n.96+163A=
ENST00000696064.1:c.-153A= ENSP00000512367.1:n.-153A=
ENST00000535573.1:n.297A=
ENST00000536076.1:n.178A=
XM_011528479.1:c.-292A= XP_011526781.1:n.-292A=