Canonical Allele Identifier: CA2365869199

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651983G= , CM000682.2:g.44651983G=	GRCh38
NC_000020.10:g.43280624G= , CM000682.1:g.43280624G=	GRCh37
NC_000020.9:g.42714038G=	NCBI36
NG_007385.1:g.4753C= , LRG_16:g.4753C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-202C=	ENSP00000512234.1:n.-202C=
ENST00000696039.1:n.240C=
ENST00000696062.1:c.96+117C=	ENSP00000512365.1:n.96+117C=
ENST00000696064.1:c.-199C=	ENSP00000512367.1:n.-199C=
ENST00000535573.1:n.251C=
ENST00000536076.1:n.132C=
XM_011528479.1:c.-338C=	XP_011526781.1:n.-338C=