Canonical Allele Identifier: CA2365869197

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651979T= , CM000682.2:g.44651979T=	GRCh38
NC_000020.10:g.43280620T= , CM000682.1:g.43280620T=	GRCh37
NC_000020.9:g.42714034T=	NCBI36
NG_007385.1:g.4757A= , LRG_16:g.4757A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-198A=	ENSP00000512234.1:n.-198A=
ENST00000696039.1:n.244A=
ENST00000696062.1:c.96+121A=	ENSP00000512365.1:n.96+121A=
ENST00000696064.1:c.-195A=	ENSP00000512367.1:n.-195A=
ENST00000535573.1:n.255A=
ENST00000536076.1:n.136A=
XM_011528479.1:c.-334A=	XP_011526781.1:n.-334A=