Canonical Allele Identifier: CA2365868990
Gene: ADA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651696C= , CM000682.2:g.44651696C= GRCh38
NC_000020.10:g.43280337C= , CM000682.1:g.43280337C= GRCh37
NC_000020.9:g.42713751C= NCBI36
NG_007385.1:g.5040G= , LRG_16:g.5040G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000492931.6:n.3G=
ENST00000536076.2:c.-121+206G= ENSP00000512234.1:n.-121+206G=
ENST00000537820.2:c.-89G= ENSP00000441818.1:n.-89G=
ENST00000695889.1:c.-89G= ENSP00000512240.1:n.-89G=
ENST00000695949.1:c.-89G= ENSP00000512281.1:n.-89G=
ENST00000695993.1:c.-89G= ENSP00000512316.1:n.-89G=
ENST00000696003.1:n.4G=
ENST00000696004.1:n.4G=
ENST00000696006.1:c.-89G= ENSP00000512325.1:n.-89G=
ENST00000696009.1:n.23G=
ENST00000696010.1:n.25G=
ENST00000696034.1:c.-89G= ENSP00000512343.1:n.-89G=
ENST00000696038.1:c.-89G= ENSP00000512344.1:n.-89G=
ENST00000696039.1:n.321+206G=
ENST00000696059.1:c.-89G= ENSP00000512362.1:n.-89G=
ENST00000696060.1:c.-89G= ENSP00000512363.1:n.-89G=
ENST00000696061.1:c.-89G= ENSP00000512364.1:n.-89G=
ENST00000696062.1:c.96+404G= ENSP00000512365.1:n.96+404G=
ENST00000696064.1:c.-118+206G= ENSP00000512367.1:n.-118+206G=
ENST00000696065.1:c.-121+206G= ENSP00000512368.1:n.-121+206G=
ENST00000696075.1:c.-89G= ENSP00000512374.1:n.-89G=
ENST00000696076.1:c.-89G= ENSP00000512375.1:n.-89G=
ENST00000696077.1:c.-89G= ENSP00000512376.1:n.-89G=
ENST00000696078.1:c.-89G= ENSP00000512377.1:n.-89G=
ENST00000696080.1:c.-89G= ENSP00000512379.1:n.-89G=
ENST00000696084.1:n.13G=
ENST00000696104.1:c.-89G= ENSP00000512399.1:n.-89G=
ENST00000696105.1:c.-89G= ENSP00000512400.1:n.-89G=
ENST00000372874.9:c.-89G= MANE Select ENSP00000361965.4:n.-89G=
ENST00000372874.8:c.-89G= ENSP00000361965.4:n.-89G=
ENST00000535573.1:n.332+206G=
ENST00000536076.1:n.213+206G=
NM_000022.2:c.-89G= , LRG_16t1:c.-89G= NP_000013.2:n.-89G=
XM_011528479.1:c.-257+206G= XP_011526781.1:n.-257+206G=
NM_000022.3:c.-89G= NP_000013.2:n.-89G=
NM_001322050.1:c.-378G= NP_001308979.1:n.-378G=
NM_001322051.1:c.-89G= NP_001308980.1:n.-89G=
NR_136160.1:n.63G=
NM_000022.4:c.-89G= MANE Select NP_000013.2:n.-89G=
NM_001322050.2:c.-378G= NP_001308979.1:n.-378G=
NM_001322051.2:c.-89G= NP_001308980.1:n.-89G=
NR_136160.2:n.4G=