Canonical Allele Identifier: CA1619397165

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039800G= , CM000668.2:g.32039800G=	GRCh38
NC_000006.11:g.32007577G= , CM000668.1:g.32007577G=	GRCh37
NC_000006.10:g.32115556G=	NCBI36
NG_007941.2:g.6493G=
NG_008337.2:g.74575C=
NG_007941.3:g.6496G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.703G= MANE Select	ENSP00000496625.1:p.Asp235=
ENST00000418967.6:c.703G=	ENSP00000408860.2:p.Asp235=
ENST00000435122.3:c.613G=	ENSP00000415043.2:p.Asp205=
ENST00000462278.1:n.392G=
ENST00000466779.5:c.*395G=	ENSP00000417321.1:n.*395G=
ENST00000466879.5:n.754G=
ENST00000479074.5:n.761G=
ENST00000479730.5:n.819G=
ENST00000483041.5:n.872G=
ENST00000486063.5:n.883G=
NM_000500.7:c.703G=	NP_000491.4:p.Asp235=
NM_001128590.3:c.613G=	NP_001122062.3:p.Asp205=
XM_011514314.1:c.298G=	XP_011512616.1:p.Asp100=
NM_000500.9:c.703G= MANE Select	NP_000491.4:p.Asp235=
NM_001368143.1:c.298G=	NP_001355072.1:p.Asp100=
NM_001368144.1:c.298G=	NP_001355073.1:p.Asp100=
NM_001128590.4:c.613G=	NP_001122062.3:p.Asp205=
NM_001368143.2:c.298G=	NP_001355072.1:p.Asp100=
NM_001368144.2:c.298G=	NP_001355073.1:p.Asp100=