Canonical Allele Identifier: CA2365869151

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651911C= , CM000682.2:g.44651911C=	GRCh38
NC_000020.10:g.43280552C= , CM000682.1:g.43280552C=	GRCh37
NC_000020.9:g.42713966C=	NCBI36
NG_007385.1:g.4825G= , LRG_16:g.4825G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-130G=	ENSP00000512234.1:n.-130G=
ENST00000696039.1:n.312G=
ENST00000696062.1:c.96+189G=	ENSP00000512365.1:n.96+189G=
ENST00000696064.1:c.-127G=	ENSP00000512367.1:n.-127G=
ENST00000696065.1:c.-130G=	ENSP00000512368.1:n.-130G=
ENST00000535573.1:n.323G=
ENST00000536076.1:n.204G=
XM_011528479.1:c.-266G=	XP_011526781.1:n.-266G=