Canonical Allele Identifier: CA1619396383
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038495C= , CM000668.2:g.32038495C= GRCh38
NC_000006.11:g.32006272C= , CM000668.1:g.32006272C= GRCh37
NC_000006.10:g.32114251C= NCBI36
NG_007941.2:g.5188C=
NG_007941.3:g.5191C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.73C= MANE Select ENSP00000496625.1:p.Leu25=
ENST00000418967.6:c.73C= ENSP00000408860.2:p.Leu25=
ENST00000435122.3:c.73C= ENSP00000415043.2:p.Leu25=
ENST00000466779.5:c.73C= ENSP00000417321.1:p.Leu25=
ENST00000469053.5:c.73C= ENSP00000418104.1:p.Leu25=
ENST00000471671.4:c.73C= ENSP00000418561.1:p.Leu25=
ENST00000478281.5:c.73C= ENSP00000419572.1:p.Leu25=
ENST00000479074.5:n.131C=
ENST00000479730.5:n.131C=
ENST00000480027.1:n.126C=
ENST00000483041.5:n.126C=
ENST00000486063.5:n.156C=
ENST00000488465.1:n.81C=
NM_000500.7:c.73C= NP_000491.4:p.Leu25=
NM_001128590.3:c.73C= NP_001122062.3:p.Leu25=
XM_011514314.1:c.-352C= XP_011512616.1:n.-352C=
NM_000500.9:c.73C= MANE Select NP_000491.4:p.Leu25=
NM_001368143.1:c.-352C= NP_001355072.1:n.-352C=
NM_001368144.1:c.-262C= NP_001355073.1:n.-262C=
NM_001128590.4:c.73C= NP_001122062.3:p.Leu25=
NM_001368143.2:c.-352C= NP_001355072.1:n.-352C=
NM_001368144.2:c.-262C= NP_001355073.1:n.-262C=