Canonical Allele Identifier: CA1619396400
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038523C= , CM000668.2:g.32038523C= GRCh38
NC_000006.11:g.32006300C= , CM000668.1:g.32006300C= GRCh37
NC_000006.10:g.32114279C= NCBI36
NG_007941.2:g.5216C=
NG_007941.3:g.5219C=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.101C= MANE Select ENSP00000496625.1:p.Ala34=
ENST00000418967.6:c.101C= ENSP00000408860.2:p.Ala34=
ENST00000435122.3:c.101C= ENSP00000415043.2:p.Ala34=
ENST00000466779.5:c.101C= ENSP00000417321.1:p.Ala34=
ENST00000469053.5:c.101C= ENSP00000418104.1:p.Ala34=
ENST00000471671.4:c.101C= ENSP00000418561.1:p.Ala34=
ENST00000478281.5:c.101C= ENSP00000419572.1:p.Ala34=
ENST00000479074.5:n.159C=
ENST00000479730.5:n.159C=
ENST00000480027.1:n.154C=
ENST00000483041.5:n.154C=
ENST00000486063.5:n.184C=
ENST00000488465.1:n.109C=
NM_000500.7:c.101C= NP_000491.4:p.Ala34=
NM_001128590.3:c.101C= NP_001122062.3:p.Ala34=
XM_011514314.1:c.-324C= XP_011512616.1:n.-324C=
NM_000500.9:c.101C= MANE Select NP_000491.4:p.Ala34=
NM_001368143.1:c.-324C= NP_001355072.1:n.-324C=
NM_001368144.1:c.-234C= NP_001355073.1:n.-234C=
NM_001128590.4:c.101C= NP_001122062.3:p.Ala34=
NM_001368143.2:c.-324C= NP_001355072.1:n.-324C=
NM_001368144.2:c.-234C= NP_001355073.1:n.-234C=