Canonical Allele Identifier: CA1619396537

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038808A= , CM000668.2:g.32038808A=	GRCh38
NC_000006.11:g.32006585A= , CM000668.1:g.32006585A=	GRCh37
NC_000006.10:g.32114564A=	NCBI36
NG_007941.2:g.5501A=
NG_007941.3:g.5504A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.289A= MANE Select	ENSP00000496625.1:p.Thr97=
ENST00000418967.6:c.289A=	ENSP00000408860.2:p.Thr97=
ENST00000435122.3:c.202+184A=	ENSP00000415043.2:n.202+184A=
ENST00000464325.5:n.226A=
ENST00000466779.5:c.289A=	ENSP00000417321.1:p.Thr97=
ENST00000466879.5:n.58A=
ENST00000469053.5:c.202+184A=	ENSP00000418104.1:n.202+184A=
ENST00000471671.4:c.289A=	ENSP00000418561.1:p.Thr97=
ENST00000478281.5:c.289A=	ENSP00000419572.1:p.Thr97=
ENST00000479074.5:n.347A=
ENST00000479730.5:n.444A=
ENST00000480027.1:n.342A=
ENST00000483041.5:n.439A=
ENST00000486063.5:n.469A=
ENST00000488465.1:n.297A=
NM_000500.7:c.289A=	NP_000491.4:p.Thr97=
NM_001128590.3:c.202+184A=	NP_001122062.3:n.202+184A=
XM_011514314.1:c.-136A=	XP_011512616.1:n.-136A=
NM_000500.9:c.289A= MANE Select	NP_000491.4:p.Thr97=
NM_001368143.1:c.-136A=	NP_001355072.1:n.-136A=
NM_001368144.1:c.-133+184A=	NP_001355073.1:n.-133+184A=
NM_001128590.4:c.202+184A=	NP_001122062.3:n.202+184A=
NM_001368143.2:c.-136A=	NP_001355072.1:n.-136A=
NM_001368144.2:c.-133+184A=	NP_001355073.1:n.-133+184A=