Canonical Allele Identifier: CA1619396540
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038811T= , CM000668.2:g.32038811T= GRCh38
NC_000006.11:g.32006588T= , CM000668.1:g.32006588T= GRCh37
NC_000006.10:g.32114567T= NCBI36
NG_007941.2:g.5504T=
NG_007941.3:g.5507T=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.292T= MANE Select ENSP00000496625.1:p.Tyr98=
ENST00000418967.6:c.292T= ENSP00000408860.2:p.Tyr98=
ENST00000435122.3:c.202+187T= ENSP00000415043.2:n.202+187T=
ENST00000464325.5:n.229T=
ENST00000466779.5:c.292T= ENSP00000417321.1:p.Ser98=
ENST00000466879.5:n.61T=
ENST00000469053.5:c.202+187T= ENSP00000418104.1:n.202+187T=
ENST00000471671.4:c.292T= ENSP00000418561.1:p.Tyr98=
ENST00000478281.5:c.292T= ENSP00000419572.1:p.Phe98=
ENST00000479074.5:n.350T=
ENST00000479730.5:n.447T=
ENST00000480027.1:n.345T=
ENST00000483041.5:n.442T=
ENST00000486063.5:n.472T=
ENST00000488465.1:n.300T=
NM_000500.7:c.292T= NP_000491.4:p.Tyr98=
NM_001128590.3:c.202+187T= NP_001122062.3:n.202+187T=
XM_011514314.1:c.-133T= XP_011512616.1:n.-133T=
NM_000500.9:c.292T= MANE Select NP_000491.4:p.Tyr98=
NM_001368143.1:c.-133T= NP_001355072.1:n.-133T=
NM_001368144.1:c.-133+187T= NP_001355073.1:n.-133+187T=
NM_001128590.4:c.202+187T= NP_001122062.3:n.202+187T=
NM_001368143.2:c.-133T= NP_001355072.1:n.-133T=
NM_001368144.2:c.-133+187T= NP_001355073.1:n.-133+187T=