Canonical Allele Identifier: CA2365869169

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651935G= , CM000682.2:g.44651935G=	GRCh38
NC_000020.10:g.43280576G= , CM000682.1:g.43280576G=	GRCh37
NC_000020.9:g.42713990G=	NCBI36
NG_007385.1:g.4801C= , LRG_16:g.4801C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-154C=	ENSP00000512234.1:n.-154C=
ENST00000696039.1:n.288C=
ENST00000696062.1:c.96+165C=	ENSP00000512365.1:n.96+165C=
ENST00000696064.1:c.-151C=	ENSP00000512367.1:n.-151C=
ENST00000535573.1:n.299C=
ENST00000536076.1:n.180C=
XM_011528479.1:c.-290C=	XP_011526781.1:n.-290C=