Canonical Allele Identifier: CA1619396771
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32039096A= , CM000668.2:g.32039096A= GRCh38
NC_000006.11:g.32006873A= , CM000668.1:g.32006873A= GRCh37
NC_000006.10:g.32114852A= NCBI36
NG_007941.2:g.5789A=
NG_007941.3:g.5792A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.295A= MANE Select ENSP00000496625.1:p.Lys99=
ENST00000418967.6:c.295A= ENSP00000408860.2:p.Lys99=
ENST00000435122.3:c.205A= ENSP00000415043.2:p.Lys69=
ENST00000464325.5:n.230-14A=
ENST00000466779.5:c.314A= ENSP00000417321.1:p.Gln105=
ENST00000466879.5:n.346A=
ENST00000469053.5:c.224A= ENSP00000418104.1:p.Gln75=
ENST00000471671.4:c.295A= ENSP00000418561.1:p.Lys99=
ENST00000478281.5:c.328A= ENSP00000419572.1:p.Lys110=
ENST00000479074.5:n.353A=
ENST00000479730.5:n.450A=
ENST00000480027.1:n.630A=
ENST00000483041.5:n.464A=
ENST00000486063.5:n.475A=
ENST00000488465.1:n.303A=
NM_000500.7:c.295A= NP_000491.4:p.Lys99=
NM_001128590.3:c.205A= NP_001122062.3:p.Lys69=
XM_011514314.1:c.-111A= XP_011512616.1:n.-111A=
NM_000500.9:c.295A= MANE Select NP_000491.4:p.Lys99=
NM_001368143.1:c.-111A= NP_001355072.1:n.-111A=
NM_001368144.1:c.-111A= NP_001355073.1:n.-111A=
NM_001128590.4:c.205A= NP_001122062.3:p.Lys69=
NM_001368143.2:c.-111A= NP_001355072.1:n.-111A=
NM_001368144.2:c.-111A= NP_001355073.1:n.-111A=