Canonical Allele Identifier: CA2365869171

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651938G= , CM000682.2:g.44651938G=	GRCh38
NC_000020.10:g.43280579G= , CM000682.1:g.43280579G=	GRCh37
NC_000020.9:g.42713993G=	NCBI36
NG_007385.1:g.4798C= , LRG_16:g.4798C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-157C=	ENSP00000512234.1:n.-157C=
ENST00000696039.1:n.285C=
ENST00000696062.1:c.96+162C=	ENSP00000512365.1:n.96+162C=
ENST00000696064.1:c.-154C=	ENSP00000512367.1:n.-154C=
ENST00000535573.1:n.296C=
ENST00000536076.1:n.177C=
XM_011528479.1:c.-293C=	XP_011526781.1:n.-293C=