Canonical Allele Identifier: CA2365869190

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651968A= , CM000682.2:g.44651968A=	GRCh38
NC_000020.10:g.43280609A= , CM000682.1:g.43280609A=	GRCh37
NC_000020.9:g.42714023A=	NCBI36
NG_007385.1:g.4768T= , LRG_16:g.4768T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-187T=	ENSP00000512234.1:n.-187T=
ENST00000696039.1:n.255T=
ENST00000696062.1:c.96+132T=	ENSP00000512365.1:n.96+132T=
ENST00000696064.1:c.-184T=	ENSP00000512367.1:n.-184T=
ENST00000535573.1:n.266T=
ENST00000536076.1:n.147T=
XM_011528479.1:c.-323T=	XP_011526781.1:n.-323T=