Canonical Allele Identifier: CA1619396903

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039329T= , CM000668.2:g.32039329T=	GRCh38
NC_000006.11:g.32007106T= , CM000668.1:g.32007106T=	GRCh37
NC_000006.10:g.32115085T=	NCBI36
NG_007941.2:g.6022T=
NG_008337.2:g.75046A=
NG_007941.3:g.6025T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.448-27T= MANE Select	ENSP00000496625.1:n.448-27T=
ENST00000418967.6:c.448-27T=	ENSP00000408860.2:n.448-27T=
ENST00000435122.3:c.358-27T=	ENSP00000415043.2:n.358-27T=
ENST00000462278.1:n.36-27T=
ENST00000464325.5:n.369-27T=
ENST00000466779.5:c.*140-27T=	ENSP00000417321.1:n.*140-27T=
ENST00000466879.5:n.499-27T=
ENST00000469053.5:c.*140-27T=	ENSP00000418104.1:n.*140-27T=
ENST00000471671.4:c.448-27T=	ENSP00000418561.1:n.448-27T=
ENST00000478281.5:c.481-27T=	ENSP00000419572.1:n.481-27T=
ENST00000479074.5:n.506-27T=
ENST00000479730.5:n.603-27T=
ENST00000483041.5:n.617-27T=
ENST00000486063.5:n.628-27T=
ENST00000488465.1:n.456-27T=
NM_000500.7:c.448-27T=	NP_000491.4:n.448-27T=
NM_001128590.3:c.358-27T=	NP_001122062.3:n.358-27T=
XM_011514314.1:c.43-27T=	XP_011512616.1:n.43-27T=
NM_000500.9:c.448-27T= MANE Select	NP_000491.4:n.448-27T=
NM_001368143.1:c.43-27T=	NP_001355072.1:n.43-27T=
NM_001368144.1:c.43-27T=	NP_001355073.1:n.43-27T=
NM_001128590.4:c.358-27T=	NP_001122062.3:n.358-27T=
NM_001368143.2:c.43-27T=	NP_001355072.1:n.43-27T=
NM_001368144.2:c.43-27T=	NP_001355073.1:n.43-27T=