Canonical Allele Identifier: CA2365869192

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651976C= , CM000682.2:g.44651976C=	GRCh38
NC_000020.10:g.43280617C= , CM000682.1:g.43280617C=	GRCh37
NC_000020.9:g.42714031C=	NCBI36
NG_007385.1:g.4760G= , LRG_16:g.4760G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-195G=	ENSP00000512234.1:n.-195G=
ENST00000696039.1:n.247G=
ENST00000696062.1:c.96+124G=	ENSP00000512365.1:n.96+124G=
ENST00000696064.1:c.-192G=	ENSP00000512367.1:n.-192G=
ENST00000535573.1:n.258G=
ENST00000536076.1:n.139G=
XM_011528479.1:c.-331G=	XP_011526781.1:n.-331G=