Canonical Allele Identifier: CA1619397309

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040088T= , CM000668.2:g.32040088T=	GRCh38
NC_000006.11:g.32007865T= , CM000668.1:g.32007865T=	GRCh37
NC_000006.10:g.32115844T=	NCBI36
NG_007941.2:g.6781T=
NG_008337.2:g.74287A=
NG_007941.3:g.6784T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.822T= MANE Select	ENSP00000496625.1:p.Ser274=
ENST00000418967.6:c.822T=	ENSP00000408860.2:p.Ser274=
ENST00000435122.3:c.732T=	ENSP00000415043.2:p.Ser244=
ENST00000479074.5:n.880T=
ENST00000479730.5:n.938T=
ENST00000483041.5:n.991T=
ENST00000486063.5:n.918+253T=
NM_000500.7:c.822T=	NP_000491.4:p.Ser274=
NM_001128590.3:c.732T=	NP_001122062.3:p.Ser244=
XM_011514314.1:c.417T=	XP_011512616.1:p.Ser139=
NM_000500.9:c.822T= MANE Select	NP_000491.4:p.Ser274=
NM_001368143.1:c.417T=	NP_001355072.1:p.Ser139=
NM_001368144.1:c.417T=	NP_001355073.1:p.Ser139=
NM_001128590.4:c.732T=	NP_001122062.3:p.Ser244=
NM_001368143.2:c.417T=	NP_001355072.1:p.Ser139=
NM_001368144.2:c.417T=	NP_001355073.1:p.Ser139=