Canonical Allele Identifier: CA1619396764

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039087C= , CM000668.2:g.32039087C=	GRCh38
NC_000006.11:g.32006864C= , CM000668.1:g.32006864C=	GRCh37
NC_000006.10:g.32114843C=	NCBI36
NG_007941.2:g.5780C=
NG_007941.3:g.5783C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.293-7C= MANE Select	ENSP00000496625.1:n.293-7C=
ENST00000418967.6:c.293-7C=	ENSP00000408860.2:n.293-7C=
ENST00000435122.3:c.203-7C=	ENSP00000415043.2:n.203-7C=
ENST00000464325.5:n.230-23C=
ENST00000466779.5:c.305C=	ENSP00000417321.1:p.Ser102=
ENST00000466879.5:n.337C=
ENST00000469053.5:c.215C=	ENSP00000418104.1:p.Ser72=
ENST00000471671.4:c.293-7C=	ENSP00000418561.1:n.293-7C=
ENST00000478281.5:c.319C=	ENSP00000419572.1:p.Pro107=
ENST00000479074.5:n.351-7C=
ENST00000479730.5:n.448-7C=
ENST00000480027.1:n.621C=
ENST00000483041.5:n.455C=
ENST00000486063.5:n.473-7C=
ENST00000488465.1:n.301-7C=
NM_000500.7:c.293-7C=	NP_000491.4:n.293-7C=
NM_001128590.3:c.203-7C=	NP_001122062.3:n.203-7C=
XM_011514314.1:c.-120C=	XP_011512616.1:n.-120C=
NM_000500.9:c.293-7C= MANE Select	NP_000491.4:n.293-7C=
NM_001368143.1:c.-120C=	NP_001355072.1:n.-120C=
NM_001368144.1:c.-120C=	NP_001355073.1:n.-120C=
NM_001128590.4:c.203-7C=	NP_001122062.3:n.203-7C=
NM_001368143.2:c.-120C=	NP_001355072.1:n.-120C=
NM_001368144.2:c.-120C=	NP_001355073.1:n.-120C=