Canonical Allele Identifier: CA2365869078

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651801C= , CM000682.2:g.44651801C=	GRCh38
NC_000020.10:g.43280442C= , CM000682.1:g.43280442C=	GRCh37
NC_000020.9:g.42713856C=	NCBI36
NG_007385.1:g.4935G= , LRG_16:g.4935G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+101G=	ENSP00000512234.1:n.-121+101G=
ENST00000696039.1:n.321+101G=
ENST00000696062.1:c.96+299G=	ENSP00000512365.1:n.96+299G=
ENST00000696064.1:c.-118+101G=	ENSP00000512367.1:n.-118+101G=
ENST00000696065.1:c.-121+101G=	ENSP00000512368.1:n.-121+101G=
ENST00000535573.1:n.332+101G=
ENST00000536076.1:n.213+101G=
XM_011528479.1:c.-257+101G=	XP_011526781.1:n.-257+101G=