Canonical Allele Identifier: CA1619396762
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32039084C= , CM000668.2:g.32039084C= GRCh38
NC_000006.11:g.32006861C= , CM000668.1:g.32006861C= GRCh37
NC_000006.10:g.32114840C= NCBI36
NG_007941.2:g.5777C=
NG_007941.3:g.5780C=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.293-10C= MANE Select ENSP00000496625.1:n.293-10C=
ENST00000418967.6:c.293-10C= ENSP00000408860.2:n.293-10C=
ENST00000435122.3:c.203-10C= ENSP00000415043.2:n.203-10C=
ENST00000464325.5:n.230-26C=
ENST00000466779.5:c.302C= ENSP00000417321.1:p.Ser101=
ENST00000466879.5:n.334C=
ENST00000469053.5:c.212C= ENSP00000418104.1:p.Ser71=
ENST00000471671.4:c.293-10C= ENSP00000418561.1:n.293-10C=
ENST00000478281.5:c.316C= ENSP00000419572.1:p.Pro106=
ENST00000479074.5:n.351-10C=
ENST00000479730.5:n.448-10C=
ENST00000480027.1:n.618C=
ENST00000483041.5:n.452C=
ENST00000486063.5:n.473-10C=
ENST00000488465.1:n.301-10C=
NM_000500.7:c.293-10C= NP_000491.4:n.293-10C=
NM_001128590.3:c.203-10C= NP_001122062.3:n.203-10C=
XM_011514314.1:c.-123C= XP_011512616.1:n.-123C=
NM_000500.9:c.293-10C= MANE Select NP_000491.4:n.293-10C=
NM_001368143.1:c.-123C= NP_001355072.1:n.-123C=
NM_001368144.1:c.-123C= NP_001355073.1:n.-123C=
NM_001128590.4:c.203-10C= NP_001122062.3:n.203-10C=
NM_001368143.2:c.-123C= NP_001355072.1:n.-123C=
NM_001368144.2:c.-123C= NP_001355073.1:n.-123C=