Canonical Allele Identifier: CA2365869195

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651978C= , CM000682.2:g.44651978C=	GRCh38
NC_000020.10:g.43280619C= , CM000682.1:g.43280619C=	GRCh37
NC_000020.9:g.42714033C=	NCBI36
NG_007385.1:g.4758G= , LRG_16:g.4758G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-197G=	ENSP00000512234.1:n.-197G=
ENST00000696039.1:n.245G=
ENST00000696062.1:c.96+122G=	ENSP00000512365.1:n.96+122G=
ENST00000696064.1:c.-194G=	ENSP00000512367.1:n.-194G=
ENST00000535573.1:n.256G=
ENST00000536076.1:n.137G=
XM_011528479.1:c.-333G=	XP_011526781.1:n.-333G=