Canonical Allele Identifier: CA2652992699

Gene: ADA

Linked Data

• gnomAD v4: 20-44651936-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651936C>A , CM000682.2:g.44651936C>A	GRCh38
NC_000020.10:g.43280577C>A , CM000682.1:g.43280577C>A	GRCh37
NC_000020.9:g.42713991C>A	NCBI36
NG_007385.1:g.4800G>T , LRG_16:g.4800G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-155G>T	ENSP00000512234.1:n.-155G>T
ENST00000696039.1:n.287G>T
ENST00000696062.1:c.96+164G>T	ENSP00000512365.1:n.96+164G>T
ENST00000696064.1:c.-152G>T	ENSP00000512367.1:n.-152G>T
ENST00000535573.1:n.298G>T
ENST00000536076.1:n.179G>T
XM_011528479.1:c.-291G>T	XP_011526781.1:n.-291G>T