Canonical Allele Identifier: CA2652992738

Gene: ADA

Linked Data

• gnomAD v4: 20-44651971-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651971C>A , CM000682.2:g.44651971C>A	GRCh38
NC_000020.10:g.43280612C>A , CM000682.1:g.43280612C>A	GRCh37
NC_000020.9:g.42714026C>A	NCBI36
NG_007385.1:g.4765G>T , LRG_16:g.4765G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-190G>T	ENSP00000512234.1:n.-190G>T
ENST00000696039.1:n.252G>T
ENST00000696062.1:c.96+129G>T	ENSP00000512365.1:n.96+129G>T
ENST00000696064.1:c.-187G>T	ENSP00000512367.1:n.-187G>T
ENST00000535573.1:n.263G>T
ENST00000536076.1:n.144G>T
XM_011528479.1:c.-326G>T	XP_011526781.1:n.-326G>T