Canonical Allele Identifier: CA1619397270
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040007G= , CM000668.2:g.32040007G= GRCh38
NC_000006.11:g.32007784G= , CM000668.1:g.32007784G= GRCh37
NC_000006.10:g.32115763G= NCBI36
NG_007941.2:g.6700G=
NG_008337.2:g.74368C=
NG_007941.3:g.6703G=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.741G= MANE Select ENSP00000496625.1:p.Glu247=
ENST00000418967.6:c.741G= ENSP00000408860.2:p.Glu247=
ENST00000435122.3:c.651G= ENSP00000415043.2:p.Glu217=
ENST00000479074.5:n.799G=
ENST00000479730.5:n.857G=
ENST00000483041.5:n.910G=
ENST00000486063.5:n.918+172G=
NM_000500.7:c.741G= NP_000491.4:p.Glu247=
NM_001128590.3:c.651G= NP_001122062.3:p.Glu217=
XM_011514314.1:c.336G= XP_011512616.1:p.Glu112=
NM_000500.9:c.741G= MANE Select NP_000491.4:p.Glu247=
NM_001368143.1:c.336G= NP_001355072.1:p.Glu112=
NM_001368144.1:c.336G= NP_001355073.1:p.Glu112=
NM_001128590.4:c.651G= NP_001122062.3:p.Glu217=
NM_001368143.2:c.336G= NP_001355072.1:p.Glu112=
NM_001368144.2:c.336G= NP_001355073.1:p.Glu112=