Canonical Allele Identifier: CA2652992701

Gene: ADA

Linked Data

• gnomAD v4: 20-44651938-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651938G>A , CM000682.2:g.44651938G>A	GRCh38
NC_000020.10:g.43280579G>A , CM000682.1:g.43280579G>A	GRCh37
NC_000020.9:g.42713993G>A	NCBI36
NG_007385.1:g.4798C>T , LRG_16:g.4798C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-157C>T	ENSP00000512234.1:n.-157C>T
ENST00000696039.1:n.285C>T
ENST00000696062.1:c.96+162C>T	ENSP00000512365.1:n.96+162C>T
ENST00000696064.1:c.-154C>T	ENSP00000512367.1:n.-154C>T
ENST00000535573.1:n.296C>T
ENST00000536076.1:n.177C>T
XM_011528479.1:c.-293C>T	XP_011526781.1:n.-293C>T