Canonical Allele Identifier: CA2652992442

Gene: ADA

Linked Data

• gnomAD v4: 20-44651705-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651705C>T , CM000682.2:g.44651705C>T	GRCh38
NC_000020.10:g.43280346C>T , CM000682.1:g.43280346C>T	GRCh37
NC_000020.9:g.42713760C>T	NCBI36
NG_007385.1:g.5031G>A , LRG_16:g.5031G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+197G>A	ENSP00000512234.1:n.-121+197G>A
ENST00000537820.2:c.-98G>A	ENSP00000441818.1:n.-98G>A
ENST00000695949.1:c.-98G>A	ENSP00000512281.1:n.-98G>A
ENST00000695993.1:c.-98G>A	ENSP00000512316.1:n.-98G>A
ENST00000696006.1:c.-98G>A	ENSP00000512325.1:n.-98G>A
ENST00000696009.1:n.14G>A
ENST00000696010.1:n.16G>A
ENST00000696039.1:n.321+197G>A
ENST00000696059.1:c.-98G>A	ENSP00000512362.1:n.-98G>A
ENST00000696060.1:c.-98G>A	ENSP00000512363.1:n.-98G>A
ENST00000696061.1:c.-98G>A	ENSP00000512364.1:n.-98G>A
ENST00000696062.1:c.96+395G>A	ENSP00000512365.1:n.96+395G>A
ENST00000696064.1:c.-118+197G>A	ENSP00000512367.1:n.-118+197G>A
ENST00000696065.1:c.-121+197G>A	ENSP00000512368.1:n.-121+197G>A
ENST00000696075.1:c.-98G>A	ENSP00000512374.1:n.-98G>A
ENST00000696076.1:c.-98G>A	ENSP00000512375.1:n.-98G>A
ENST00000696077.1:c.-98G>A	ENSP00000512376.1:n.-98G>A
ENST00000696078.1:c.-98G>A	ENSP00000512377.1:n.-98G>A
ENST00000696080.1:c.-98G>A	ENSP00000512379.1:n.-98G>A
ENST00000696084.1:n.4G>A
ENST00000372874.8:c.-98G>A	ENSP00000361965.4:n.-98G>A
ENST00000535573.1:n.332+197G>A
ENST00000536076.1:n.213+197G>A
NM_000022.2:c.-98G>A , LRG_16t1:c.-98G>A	NP_000013.2:n.-98G>A
XM_011528479.1:c.-257+197G>A	XP_011526781.1:n.-257+197G>A
NM_000022.3:c.-98G>A	NP_000013.2:n.-98G>A
NM_001322050.1:c.-387G>A	NP_001308979.1:n.-387G>A
NM_001322051.1:c.-98G>A	NP_001308980.1:n.-98G>A
NR_136160.1:n.54G>A