Canonical Allele Identifier: CA2365869185

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651958A= , CM000682.2:g.44651958A=	GRCh38
NC_000020.10:g.43280599A= , CM000682.1:g.43280599A=	GRCh37
NC_000020.9:g.42714013A=	NCBI36
NG_007385.1:g.4778T= , LRG_16:g.4778T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-177T=	ENSP00000512234.1:n.-177T=
ENST00000696039.1:n.265T=
ENST00000696062.1:c.96+142T=	ENSP00000512365.1:n.96+142T=
ENST00000696064.1:c.-174T=	ENSP00000512367.1:n.-174T=
ENST00000535573.1:n.276T=
ENST00000536076.1:n.157T=
XM_011528479.1:c.-313T=	XP_011526781.1:n.-313T=