Canonical Allele Identifier: CA2365869168

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651934C= , CM000682.2:g.44651934C=	GRCh38
NC_000020.10:g.43280575C= , CM000682.1:g.43280575C=	GRCh37
NC_000020.9:g.42713989C=	NCBI36
NG_007385.1:g.4802G= , LRG_16:g.4802G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-153G=	ENSP00000512234.1:n.-153G=
ENST00000696039.1:n.289G=
ENST00000696062.1:c.96+166G=	ENSP00000512365.1:n.96+166G=
ENST00000696064.1:c.-150G=	ENSP00000512367.1:n.-150G=
ENST00000535573.1:n.300G=
ENST00000536076.1:n.181G=
XM_011528479.1:c.-289G=	XP_011526781.1:n.-289G=