Canonical Allele Identifier: CA1619396625

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038917C= , CM000668.2:g.32038917C=	GRCh38
NC_000006.11:g.32006694C= , CM000668.1:g.32006694C=	GRCh37
NC_000006.10:g.32114673C=	NCBI36
NG_007941.2:g.5610C=
NG_007941.3:g.5613C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.292+106C= MANE Select	ENSP00000496625.1:n.292+106C=
ENST00000418967.6:c.292+106C=	ENSP00000408860.2:n.292+106C=
ENST00000435122.3:c.203-177C=	ENSP00000415043.2:n.203-177C=
ENST00000464325.5:n.229+106C=
ENST00000466779.5:c.292+106C=	ENSP00000417321.1:n.292+106C=
ENST00000466879.5:n.167C=
ENST00000469053.5:c.203-158C=	ENSP00000418104.1:n.203-158C=
ENST00000471671.4:c.292+106C=	ENSP00000418561.1:n.292+106C=
ENST00000478281.5:c.292+106C=	ENSP00000419572.1:n.292+106C=
ENST00000479074.5:n.350+106C=
ENST00000479730.5:n.447+106C=
ENST00000480027.1:n.451C=
ENST00000483041.5:n.442+106C=
ENST00000486063.5:n.472+106C=
ENST00000488465.1:n.300+106C=
NM_000500.7:c.292+106C=	NP_000491.4:n.292+106C=
NM_001128590.3:c.203-177C=	NP_001122062.3:n.203-177C=
XM_011514314.1:c.-133+106C=	XP_011512616.1:n.-133+106C=
NM_000500.9:c.292+106C= MANE Select	NP_000491.4:n.292+106C=
NM_001368143.1:c.-133+106C=	NP_001355072.1:n.-133+106C=
NM_001368144.1:c.-132-158C=	NP_001355073.1:n.-132-158C=
NM_001128590.4:c.203-177C=	NP_001122062.3:n.203-177C=
NM_001368143.2:c.-133+106C=	NP_001355072.1:n.-133+106C=
NM_001368144.2:c.-132-158C=	NP_001355073.1:n.-132-158C=