Canonical Allele Identifier: CA2365869119

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651856C= , CM000682.2:g.44651856C=	GRCh38
NC_000020.10:g.43280497C= , CM000682.1:g.43280497C=	GRCh37
NC_000020.9:g.42713911C=	NCBI36
NG_007385.1:g.4880G= , LRG_16:g.4880G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+46G=	ENSP00000512234.1:n.-121+46G=
ENST00000696039.1:n.321+46G=
ENST00000696062.1:c.96+244G=	ENSP00000512365.1:n.96+244G=
ENST00000696064.1:c.-118+46G=	ENSP00000512367.1:n.-118+46G=
ENST00000696065.1:c.-121+46G=	ENSP00000512368.1:n.-121+46G=
ENST00000535573.1:n.332+46G=
ENST00000536076.1:n.213+46G=
XM_011528479.1:c.-257+46G=	XP_011526781.1:n.-257+46G=