Canonical Allele Identifier: CA2652992436

Gene: ADA

Linked Data

• gnomAD v4: 20-44651703-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651703G>A , CM000682.2:g.44651703G>A	GRCh38
NC_000020.10:g.43280344G>A , CM000682.1:g.43280344G>A	GRCh37
NC_000020.9:g.42713758G>A	NCBI36
NG_007385.1:g.5033C>T , LRG_16:g.5033C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+199C>T	ENSP00000512234.1:n.-121+199C>T
ENST00000537820.2:c.-96C>T	ENSP00000441818.1:n.-96C>T
ENST00000695889.1:c.-96C>T	ENSP00000512240.1:n.-96C>T
ENST00000695949.1:c.-96C>T	ENSP00000512281.1:n.-96C>T
ENST00000695993.1:c.-96C>T	ENSP00000512316.1:n.-96C>T
ENST00000696006.1:c.-96C>T	ENSP00000512325.1:n.-96C>T
ENST00000696009.1:n.16C>T
ENST00000696010.1:n.18C>T
ENST00000696039.1:n.321+199C>T
ENST00000696059.1:c.-96C>T	ENSP00000512362.1:n.-96C>T
ENST00000696060.1:c.-96C>T	ENSP00000512363.1:n.-96C>T
ENST00000696061.1:c.-96C>T	ENSP00000512364.1:n.-96C>T
ENST00000696062.1:c.96+397C>T	ENSP00000512365.1:n.96+397C>T
ENST00000696064.1:c.-118+199C>T	ENSP00000512367.1:n.-118+199C>T
ENST00000696065.1:c.-121+199C>T	ENSP00000512368.1:n.-121+199C>T
ENST00000696075.1:c.-96C>T	ENSP00000512374.1:n.-96C>T
ENST00000696076.1:c.-96C>T	ENSP00000512375.1:n.-96C>T
ENST00000696077.1:c.-96C>T	ENSP00000512376.1:n.-96C>T
ENST00000696078.1:c.-96C>T	ENSP00000512377.1:n.-96C>T
ENST00000696080.1:c.-96C>T	ENSP00000512379.1:n.-96C>T
ENST00000696084.1:n.6C>T
ENST00000372874.8:c.-96C>T	ENSP00000361965.4:n.-96C>T
ENST00000535573.1:n.332+199C>T
ENST00000536076.1:n.213+199C>T
NM_000022.2:c.-96C>T , LRG_16t1:c.-96C>T	NP_000013.2:n.-96C>T
XM_011528479.1:c.-257+199C>T	XP_011526781.1:n.-257+199C>T
NM_000022.3:c.-96C>T	NP_000013.2:n.-96C>T
NM_001322050.1:c.-385C>T	NP_001308979.1:n.-385C>T
NM_001322051.1:c.-96C>T	NP_001308980.1:n.-96C>T
NR_136160.1:n.56C>T