Canonical Allele Identifier: CA2652992627

Gene: ADA

Linked Data

• gnomAD v4: 20-44651873-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651873A>C , CM000682.2:g.44651873A>C	GRCh38
NC_000020.10:g.43280514A>C , CM000682.1:g.43280514A>C	GRCh37
NC_000020.9:g.42713928A>C	NCBI36
NG_007385.1:g.4863T>G , LRG_16:g.4863T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+29T>G	ENSP00000512234.1:n.-121+29T>G
ENST00000696039.1:n.321+29T>G
ENST00000696062.1:c.96+227T>G	ENSP00000512365.1:n.96+227T>G
ENST00000696064.1:c.-118+29T>G	ENSP00000512367.1:n.-118+29T>G
ENST00000696065.1:c.-121+29T>G	ENSP00000512368.1:n.-121+29T>G
ENST00000535573.1:n.332+29T>G
ENST00000536076.1:n.213+29T>G
XM_011528479.1:c.-257+29T>G	XP_011526781.1:n.-257+29T>G