Canonical Allele Identifier: CA1619396536
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038807T= , CM000668.2:g.32038807T= GRCh38
NC_000006.11:g.32006584T= , CM000668.1:g.32006584T= GRCh37
NC_000006.10:g.32114563T= NCBI36
NG_007941.2:g.5500T=
NG_007941.3:g.5503T=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.288T= MANE Select ENSP00000496625.1:p.Leu96=
ENST00000418967.6:c.288T= ENSP00000408860.2:p.Leu96=
ENST00000435122.3:c.202+183T= ENSP00000415043.2:n.202+183T=
ENST00000464325.5:n.225T=
ENST00000466779.5:c.288T= ENSP00000417321.1:p.Leu96=
ENST00000466879.5:n.57T=
ENST00000469053.5:c.202+183T= ENSP00000418104.1:n.202+183T=
ENST00000471671.4:c.288T= ENSP00000418561.1:p.Leu96=
ENST00000478281.5:c.288T= ENSP00000419572.1:p.Leu96=
ENST00000479074.5:n.346T=
ENST00000479730.5:n.443T=
ENST00000480027.1:n.341T=
ENST00000483041.5:n.438T=
ENST00000486063.5:n.468T=
ENST00000488465.1:n.296T=
NM_000500.7:c.288T= NP_000491.4:p.Leu96=
NM_001128590.3:c.202+183T= NP_001122062.3:n.202+183T=
XM_011514314.1:c.-137T= XP_011512616.1:n.-137T=
NM_000500.9:c.288T= MANE Select NP_000491.4:p.Leu96=
NM_001368143.1:c.-137T= NP_001355072.1:n.-137T=
NM_001368144.1:c.-133+183T= NP_001355073.1:n.-133+183T=
NM_001128590.4:c.202+183T= NP_001122062.3:n.202+183T=
NM_001368143.2:c.-137T= NP_001355072.1:n.-137T=
NM_001368144.2:c.-133+183T= NP_001355073.1:n.-133+183T=