Canonical Allele Identifier: CA2365869066

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651785C= , CM000682.2:g.44651785C=	GRCh38
NC_000020.10:g.43280426C= , CM000682.1:g.43280426C=	GRCh37
NC_000020.9:g.42713840C=	NCBI36
NG_007385.1:g.4951G= , LRG_16:g.4951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+117G=	ENSP00000512234.1:n.-121+117G=
ENST00000696039.1:n.321+117G=
ENST00000696062.1:c.96+315G=	ENSP00000512365.1:n.96+315G=
ENST00000696064.1:c.-118+117G=	ENSP00000512367.1:n.-118+117G=
ENST00000696065.1:c.-121+117G=	ENSP00000512368.1:n.-121+117G=
ENST00000535573.1:n.332+117G=
ENST00000536076.1:n.213+117G=
XM_011528479.1:c.-257+117G=	XP_011526781.1:n.-257+117G=