Canonical Allele Identifier: CA2365869145

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651903T= , CM000682.2:g.44651903T=	GRCh38
NC_000020.10:g.43280544T= , CM000682.1:g.43280544T=	GRCh37
NC_000020.9:g.42713958T=	NCBI36
NG_007385.1:g.4833A= , LRG_16:g.4833A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-122A=	ENSP00000512234.1:n.-122A=
ENST00000696039.1:n.320A=
ENST00000696062.1:c.96+197A=	ENSP00000512365.1:n.96+197A=
ENST00000696064.1:c.-119A=	ENSP00000512367.1:n.-119A=
ENST00000696065.1:c.-122A=	ENSP00000512368.1:n.-122A=
ENST00000535573.1:n.331A=
ENST00000536076.1:n.212A=
XM_011528479.1:c.-258A=	XP_011526781.1:n.-258A=