Canonical Allele Identifier: CA2365869172

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651942T= , CM000682.2:g.44651942T=	GRCh38
NC_000020.10:g.43280583T= , CM000682.1:g.43280583T=	GRCh37
NC_000020.9:g.42713997T=	NCBI36
NG_007385.1:g.4794A= , LRG_16:g.4794A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-161A=	ENSP00000512234.1:n.-161A=
ENST00000696039.1:n.281A=
ENST00000696062.1:c.96+158A=	ENSP00000512365.1:n.96+158A=
ENST00000696064.1:c.-158A=	ENSP00000512367.1:n.-158A=
ENST00000535573.1:n.292A=
ENST00000536076.1:n.173A=
XM_011528479.1:c.-297A=	XP_011526781.1:n.-297A=