Canonical Allele Identifier: CA1619396916
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32039356C= , CM000668.2:g.32039356C= GRCh38
NC_000006.11:g.32007133C= , CM000668.1:g.32007133C= GRCh37
NC_000006.10:g.32115112C= NCBI36
NG_007941.2:g.6049C=
NG_008337.2:g.75019G=
NG_007941.3:g.6052C=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.448C= MANE Select ENSP00000496625.1:p.Arg150=
ENST00000418967.6:c.448C= ENSP00000408860.2:p.Arg150=
ENST00000435122.3:c.358C= ENSP00000415043.2:p.Arg120=
ENST00000462278.1:n.36C=
ENST00000464325.5:n.369C=
ENST00000466779.5:c.*140C= ENSP00000417321.1:n.*140C=
ENST00000466879.5:n.499C=
ENST00000469053.5:c.*140C= ENSP00000418104.1:n.*140C=
ENST00000471671.4:c.448C= ENSP00000418561.1:p.Arg150=
ENST00000478281.5:c.481C= ENSP00000419572.1:p.Arg161=
ENST00000479074.5:n.506C=
ENST00000479730.5:n.603C=
ENST00000483041.5:n.617C=
ENST00000486063.5:n.628C=
ENST00000488465.1:n.456C=
NM_000500.7:c.448C= NP_000491.4:p.Arg150=
NM_001128590.3:c.358C= NP_001122062.3:p.Arg120=
XM_011514314.1:c.43C= XP_011512616.1:p.Arg15=
NM_000500.9:c.448C= MANE Select NP_000491.4:p.Arg150=
NM_001368143.1:c.43C= NP_001355072.1:p.Arg15=
NM_001368144.1:c.43C= NP_001355073.1:p.Arg15=
NM_001128590.4:c.358C= NP_001122062.3:p.Arg120=
NM_001368143.2:c.43C= NP_001355072.1:p.Arg15=
NM_001368144.2:c.43C= NP_001355073.1:p.Arg15=