Canonical Allele Identifier: CA2652992717

Gene: ADA

Linked Data

• gnomAD v4: 20-44651950-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651950G>T , CM000682.2:g.44651950G>T	GRCh38
NC_000020.10:g.43280591G>T , CM000682.1:g.43280591G>T	GRCh37
NC_000020.9:g.42714005G>T	NCBI36
NG_007385.1:g.4786C>A , LRG_16:g.4786C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-169C>A	ENSP00000512234.1:n.-169C>A
ENST00000696039.1:n.273C>A
ENST00000696062.1:c.96+150C>A	ENSP00000512365.1:n.96+150C>A
ENST00000696064.1:c.-166C>A	ENSP00000512367.1:n.-166C>A
ENST00000535573.1:n.284C>A
ENST00000536076.1:n.165C>A
XM_011528479.1:c.-305C>A	XP_011526781.1:n.-305C>A