Canonical Allele Identifier: CA2652992691

Gene: ADA

Linked Data

• gnomAD v4: 20-44651928-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651928G>A , CM000682.2:g.44651928G>A	GRCh38
NC_000020.10:g.43280569G>A , CM000682.1:g.43280569G>A	GRCh37
NC_000020.9:g.42713983G>A	NCBI36
NG_007385.1:g.4808C>T , LRG_16:g.4808C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-147C>T	ENSP00000512234.1:n.-147C>T
ENST00000696039.1:n.295C>T
ENST00000696062.1:c.96+172C>T	ENSP00000512365.1:n.96+172C>T
ENST00000696064.1:c.-144C>T	ENSP00000512367.1:n.-144C>T
ENST00000535573.1:n.306C>T
ENST00000536076.1:n.187C>T
XM_011528479.1:c.-283C>T	XP_011526781.1:n.-283C>T