Canonical Allele Identifier: CA1619396337
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038419C= , CM000668.2:g.32038419C= GRCh38
NC_000006.11:g.32006196C= , CM000668.1:g.32006196C= GRCh37
NC_000006.10:g.32114175C= NCBI36
NG_007941.2:g.5115C=
NG_007941.3:g.5115C=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.-4C= MANE Select ENSP00000496625.1:n.-4C=
ENST00000418967.6:c.-4C= ENSP00000408860.2:n.-4C=
ENST00000435122.3:c.-4C= ENSP00000415043.2:n.-4C=
ENST00000466779.5:c.-4C= ENSP00000417321.1:n.-4C=
ENST00000469053.5:c.-4C= ENSP00000418104.1:n.-4C=
ENST00000471671.4:c.-4C= ENSP00000418561.1:n.-4C=
ENST00000478281.5:c.-4C= ENSP00000419572.1:n.-4C=
ENST00000479074.5:n.55C=
ENST00000479730.5:n.55C=
ENST00000480027.1:n.50C=
ENST00000483041.5:n.50C=
ENST00000486063.5:n.80C=
ENST00000488465.1:n.5C=
NM_000500.7:c.-4C= NP_000491.4:n.-4C=
NM_001128590.3:c.-4C= NP_001122062.3:n.-4C=
XM_011514314.1:c.-428C= XP_011512616.1:n.-428C=
NM_000500.9:c.-4C= MANE Select NP_000491.4:n.-4C=
NM_001368143.1:c.-428C= NP_001355072.1:n.-428C=
NM_001368144.1:c.-338C= NP_001355073.1:n.-338C=
NM_001128590.4:c.-4C= NP_001122062.3:n.-4C=
NM_001368143.2:c.-428C= NP_001355072.1:n.-428C=
NM_001368144.2:c.-338C= NP_001355073.1:n.-338C=