Canonical Allele Identifier: CA1619396919
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32039362A= , CM000668.2:g.32039362A= GRCh38
NC_000006.11:g.32007139A= , CM000668.1:g.32007139A= GRCh37
NC_000006.10:g.32115118A= NCBI36
NG_007941.2:g.6055A=
NG_008337.2:g.75013T=
NG_007941.3:g.6058A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.454A= MANE Select ENSP00000496625.1:p.Arg152=
ENST00000418967.6:c.454A= ENSP00000408860.2:p.Arg152=
ENST00000435122.3:c.364A= ENSP00000415043.2:p.Arg122=
ENST00000462278.1:n.42A=
ENST00000464325.5:n.375A=
ENST00000466779.5:c.*146A= ENSP00000417321.1:n.*146A=
ENST00000466879.5:n.505A=
ENST00000469053.5:c.*146A= ENSP00000418104.1:n.*146A=
ENST00000471671.4:c.454A= ENSP00000418561.1:p.Arg152=
ENST00000478281.5:c.487A= ENSP00000419572.1:p.Arg163=
ENST00000479074.5:n.512A=
ENST00000479730.5:n.609A=
ENST00000483041.5:n.623A=
ENST00000486063.5:n.634A=
ENST00000488465.1:n.462A=
NM_000500.7:c.454A= NP_000491.4:p.Arg152=
NM_001128590.3:c.364A= NP_001122062.3:p.Arg122=
XM_011514314.1:c.49A= XP_011512616.1:p.Arg17=
NM_000500.9:c.454A= MANE Select NP_000491.4:p.Arg152=
NM_001368143.1:c.49A= NP_001355072.1:p.Arg17=
NM_001368144.1:c.49A= NP_001355073.1:p.Arg17=
NM_001128590.4:c.364A= NP_001122062.3:p.Arg122=
NM_001368143.2:c.49A= NP_001355072.1:p.Arg17=
NM_001368144.2:c.49A= NP_001355073.1:p.Arg17=