Canonical Allele Identifier: CA1619396534
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038800A= , CM000668.2:g.32038800A= GRCh38
NC_000006.11:g.32006577A= , CM000668.1:g.32006577A= GRCh37
NC_000006.10:g.32114556A= NCBI36
NG_007941.2:g.5493A=
NG_007941.3:g.5496A=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.281A= MANE Select ENSP00000496625.1:p.Glu94=
ENST00000418967.6:c.281A= ENSP00000408860.2:p.Glu94=
ENST00000435122.3:c.202+176A= ENSP00000415043.2:n.202+176A=
ENST00000464325.5:n.218A=
ENST00000466779.5:c.281A= ENSP00000417321.1:p.Glu94=
ENST00000466879.5:n.50A=
ENST00000469053.5:c.202+176A= ENSP00000418104.1:n.202+176A=
ENST00000471671.4:c.281A= ENSP00000418561.1:p.Glu94=
ENST00000478281.5:c.281A= ENSP00000419572.1:p.Glu94=
ENST00000479074.5:n.339A=
ENST00000479730.5:n.436A=
ENST00000480027.1:n.334A=
ENST00000483041.5:n.431A=
ENST00000486063.5:n.461A=
ENST00000488465.1:n.289A=
NM_000500.7:c.281A= NP_000491.4:p.Glu94=
NM_001128590.3:c.202+176A= NP_001122062.3:n.202+176A=
XM_011514314.1:c.-144A= XP_011512616.1:n.-144A=
NM_000500.9:c.281A= MANE Select NP_000491.4:p.Glu94=
NM_001368143.1:c.-144A= NP_001355072.1:n.-144A=
NM_001368144.1:c.-133+176A= NP_001355073.1:n.-133+176A=
NM_001128590.4:c.202+176A= NP_001122062.3:n.202+176A=
NM_001368143.2:c.-144A= NP_001355072.1:n.-144A=
NM_001368144.2:c.-133+176A= NP_001355073.1:n.-133+176A=