Canonical Allele Identifier: CA2652992702

Gene: ADA

Linked Data

• gnomAD v4: 20-44651939-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651939C>A , CM000682.2:g.44651939C>A	GRCh38
NC_000020.10:g.43280580C>A , CM000682.1:g.43280580C>A	GRCh37
NC_000020.9:g.42713994C>A	NCBI36
NG_007385.1:g.4797G>T , LRG_16:g.4797G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-158G>T	ENSP00000512234.1:n.-158G>T
ENST00000696039.1:n.284G>T
ENST00000696062.1:c.96+161G>T	ENSP00000512365.1:n.96+161G>T
ENST00000696064.1:c.-155G>T	ENSP00000512367.1:n.-155G>T
ENST00000535573.1:n.295G>T
ENST00000536076.1:n.176G>T
XM_011528479.1:c.-294G>T	XP_011526781.1:n.-294G>T