Canonical Allele Identifier: CA14809107
Gene: ADA HGNC NCBI

Linked Data

dbSNP Id: rs244072

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44630665A>G , CM000682.2:g.44630665A>G GRCh38
NC_000020.10:g.43259306A>G , CM000682.1:g.43259306A>G GRCh37
NC_000020.9:g.42692720A>G NCBI36
NG_007385.1:g.26071T>C , LRG_16:g.26071T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372874.9:c.96-1496T>C MANE Select ENSP00000361965.4:p.=
ENST00000372874.8:c.96-1496T>C ENSP00000361965.4:p.=
ENST00000492931.5:n.180-1496T>C
ENST00000536076.1:n.276-1496T>C
ENST00000536532.5:c.96-1496T>C ENSP00000440946.1:p.=
ENST00000537820.1:c.96-1496T>C ENSP00000441818.1:p.=
ENST00000539235.5:c.96-1496T>C ENSP00000446464.1:p.=
ENST00000545776.5:n.150-1496T>C
NM_000022.2:c.96-1496T>C , LRG_16t1:c.96-1496T>C NP_000013.2:p.=
XM_005260236.2:c.96-1496T>C XP_005260293.1:p.=
XM_011528478.1:c.-194-1496T>C XP_011526780.1:p.=
XM_011528479.1:c.-194-1496T>C XP_011526781.1:p.=
XR_244129.1:n.150-1496T>C
NM_000022.3:c.96-1496T>C NP_000013.2:p.=
NM_001322050.1:c.-194-1496T>C NP_001308979.1:p.=
NM_001322051.1:c.96-1496T>C NP_001308980.1:p.=
NR_136160.1:n.247-1496T>C
NM_000022.4:c.96-1496T>C MANE Select NP_000013.2:p.=
NM_001322050.2:c.-194-1496T>C NP_001308979.1:p.=
NM_001322051.2:c.96-1496T>C NP_001308980.1:p.=
NR_136160.2:n.188-1496T>C