Canonical Allele Identifier: CA1619396846
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32039243T= , CM000668.2:g.32039243T= GRCh38
NC_000006.11:g.32007020T= , CM000668.1:g.32007020T= GRCh37
NC_000006.10:g.32114999T= NCBI36
NG_007941.2:g.5936T=
NG_008337.2:g.75132A=
NG_007941.3:g.5939T=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.442T= MANE Select ENSP00000496625.1:p.Cys148=
ENST00000418967.6:c.442T= ENSP00000408860.2:p.Cys148=
ENST00000435122.3:c.352T= ENSP00000415043.2:p.Cys118=
ENST00000462278.1:n.30T=
ENST00000464325.5:n.363T=
ENST00000466779.5:c.*134T= ENSP00000417321.1:n.*134T=
ENST00000466879.5:n.493T=
ENST00000469053.5:c.*134T= ENSP00000418104.1:n.*134T=
ENST00000471671.4:c.442T= ENSP00000418561.1:p.Cys148=
ENST00000478281.5:c.475T= ENSP00000419572.1:p.Cys159=
ENST00000479074.5:n.500T=
ENST00000479730.5:n.597T=
ENST00000483041.5:n.611T=
ENST00000486063.5:n.622T=
ENST00000488465.1:n.450T=
NM_000500.7:c.442T= NP_000491.4:p.Cys148=
NM_001128590.3:c.352T= NP_001122062.3:p.Cys118=
XM_011514314.1:c.37T= XP_011512616.1:p.Cys13=
NM_000500.9:c.442T= MANE Select NP_000491.4:p.Cys148=
NM_001368143.1:c.37T= NP_001355072.1:p.Cys13=
NM_001368144.1:c.37T= NP_001355073.1:p.Cys13=
NM_001128590.4:c.352T= NP_001122062.3:p.Cys118=
NM_001368143.2:c.37T= NP_001355072.1:p.Cys13=
NM_001368144.2:c.37T= NP_001355073.1:p.Cys13=