Canonical Allele Identifier: CA2652992745

Gene: ADA

Linked Data

• gnomAD v4: 20-44651979-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651979T>A , CM000682.2:g.44651979T>A	GRCh38
NC_000020.10:g.43280620T>A , CM000682.1:g.43280620T>A	GRCh37
NC_000020.9:g.42714034T>A	NCBI36
NG_007385.1:g.4757A>T , LRG_16:g.4757A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-198A>T	ENSP00000512234.1:n.-198A>T
ENST00000696039.1:n.244A>T
ENST00000696062.1:c.96+121A>T	ENSP00000512365.1:n.96+121A>T
ENST00000696064.1:c.-195A>T	ENSP00000512367.1:n.-195A>T
ENST00000535573.1:n.255A>T
ENST00000536076.1:n.136A>T
XM_011528479.1:c.-334A>T	XP_011526781.1:n.-334A>T