Canonical Allele Identifier: CA2678088391
Gene: CYP21A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038797del , CM000668.2:g.32038797del GRCh38
NC_000006.11:g.32006574del , CM000668.1:g.32006574del GRCh37
NC_000006.10:g.32114553del NCBI36
NG_007941.2:g.5490del
NG_007941.3:g.5493del

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.278del MANE Select ENSP00000496625.1:p.Pro93LeufsTer?
ENST00000418967.6:c.278del ENSP00000408860.2:p.Pro93LeufsTer?
ENST00000435122.3:c.202+173del ENSP00000415043.2:n.202+173del
ENST00000464325.5:n.215del
ENST00000466779.5:c.278del ENSP00000417321.1:p.Pro93LeufsTer?
ENST00000466879.5:n.47del
ENST00000469053.5:c.202+173del ENSP00000418104.1:n.202+173del
ENST00000471671.4:c.278del ENSP00000418561.1:p.Pro93LeufsTer?
ENST00000478281.5:c.278del ENSP00000419572.1:p.Pro93LeufsTer?
ENST00000479074.5:n.336del
ENST00000479730.5:n.433del
ENST00000480027.1:n.331del
ENST00000483041.5:n.428del
ENST00000486063.5:n.458del
ENST00000488465.1:n.286del
NM_000500.7:c.278del NP_000491.4:p.Pro93LeufsTer?
NM_001128590.3:c.202+173del NP_001122062.3:n.202+173del
XM_011514314.1:c.-147del XP_011512616.1:n.-147del
NM_000500.9:c.278del MANE Select NP_000491.4:p.Pro93LeufsTer?
NM_001368143.1:c.-147del NP_001355072.1:n.-147del
NM_001368144.1:c.-133+173del NP_001355073.1:n.-133+173del
NM_001128590.4:c.202+173del NP_001122062.3:n.202+173del
NM_001368143.2:c.-147del NP_001355072.1:n.-147del
NM_001368144.2:c.-133+173del NP_001355073.1:n.-133+173del