Canonical Allele Identifier: CA1619396463
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038656A= , CM000668.2:g.32038656A= GRCh38
NC_000006.11:g.32006433A= , CM000668.1:g.32006433A= GRCh37
NC_000006.10:g.32114412A= NCBI36
NG_007941.2:g.5349A=
NG_007941.3:g.5352A=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.202+32A= MANE Select ENSP00000496625.1:n.202+32A=
ENST00000418967.6:c.202+32A= ENSP00000408860.2:n.202+32A=
ENST00000435122.3:c.202+32A= ENSP00000415043.2:n.202+32A=
ENST00000464325.5:n.74A=
ENST00000466779.5:c.202+32A= ENSP00000417321.1:n.202+32A=
ENST00000469053.5:c.202+32A= ENSP00000418104.1:n.202+32A=
ENST00000471671.4:c.202+32A= ENSP00000418561.1:n.202+32A=
ENST00000478281.5:c.202+32A= ENSP00000419572.1:n.202+32A=
ENST00000479074.5:n.260+32A=
ENST00000479730.5:n.292A=
ENST00000480027.1:n.255+32A=
ENST00000483041.5:n.287A=
ENST00000486063.5:n.317A=
ENST00000488465.1:n.210+32A=
NM_000500.7:c.202+32A= NP_000491.4:n.202+32A=
NM_001128590.3:c.202+32A= NP_001122062.3:n.202+32A=
XM_011514314.1:c.-223+32A= XP_011512616.1:n.-223+32A=
NM_000500.9:c.202+32A= MANE Select NP_000491.4:n.202+32A=
NM_001368143.1:c.-223+32A= NP_001355072.1:n.-223+32A=
NM_001368144.1:c.-133+32A= NP_001355073.1:n.-133+32A=
NM_001128590.4:c.202+32A= NP_001122062.3:n.202+32A=
NM_001368143.2:c.-223+32A= NP_001355072.1:n.-223+32A=
NM_001368144.2:c.-133+32A= NP_001355073.1:n.-133+32A=