Canonical Allele Identifier: CA2652992754

Gene: ADA

Linked Data

• gnomAD v4: 20-44651991-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651991G>A , CM000682.2:g.44651991G>A	GRCh38
NC_000020.10:g.43280632G>A , CM000682.1:g.43280632G>A	GRCh37
NC_000020.9:g.42714046G>A	NCBI36
NG_007385.1:g.4745C>T , LRG_16:g.4745C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-210C>T	ENSP00000512234.1:n.-210C>T
ENST00000696039.1:n.232C>T
ENST00000696062.1:c.96+109C>T	ENSP00000512365.1:n.96+109C>T
ENST00000696064.1:c.-207C>T	ENSP00000512367.1:n.-207C>T
ENST00000535573.1:n.243C>T
ENST00000536076.1:n.124C>T
XM_011528479.1:c.-346C>T	XP_011526781.1:n.-346C>T