Canonical Allele Identifier: CA1619399247
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040485G= , CM000668.2:g.32040485G= GRCh38
NC_000006.11:g.32008262G= , CM000668.1:g.32008262G= GRCh37
NC_000006.10:g.32116241G= NCBI36
NG_007941.2:g.7178G=
NG_008337.2:g.73890C=
NG_007941.3:g.7181G=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.1019G= MANE Select ENSP00000496625.1:p.Arg340=
ENST00000418967.6:c.1019G= ENSP00000408860.2:p.Arg340=
ENST00000435122.3:c.929G= ENSP00000415043.2:p.Arg310=
ENST00000479074.5:n.1077G=
ENST00000479730.5:n.1135G=
ENST00000483041.5:n.1188G=
ENST00000486063.5:n.998G=
NM_000500.7:c.1019G= NP_000491.4:p.Arg340=
NM_001128590.3:c.929G= NP_001122062.3:p.Arg310=
XM_011514314.1:c.614G= XP_011512616.1:p.Arg205=
NM_000500.9:c.1019G= MANE Select NP_000491.4:p.Arg340=
NM_001368143.1:c.614G= NP_001355072.1:p.Arg205=
NM_001368144.1:c.614G= NP_001355073.1:p.Arg205=
NM_001128590.4:c.929G= NP_001122062.3:p.Arg310=
NM_001368143.2:c.614G= NP_001355072.1:p.Arg205=
NM_001368144.2:c.614G= NP_001355073.1:p.Arg205=