Canonical Allele Identifier: CA1619397070

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039610G= , CM000668.2:g.32039610G=	GRCh38
NC_000006.11:g.32007387G= , CM000668.1:g.32007387G=	GRCh37
NC_000006.10:g.32115366G=	NCBI36
NG_007941.2:g.6303G=
NG_008337.2:g.74765C=
NG_007941.3:g.6306G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.614G= MANE Select	ENSP00000496625.1:p.Trp205=
ENST00000418967.6:c.614G=	ENSP00000408860.2:p.Trp205=
ENST00000435122.3:c.524G=	ENSP00000415043.2:p.Trp175=
ENST00000462278.1:n.202G=
ENST00000464325.5:n.535G=
ENST00000466779.5:c.*306G=	ENSP00000417321.1:n.*306G=
ENST00000466879.5:n.665G=
ENST00000469053.5:c.*306G=	ENSP00000418104.1:n.*306G=
ENST00000479074.5:n.672G=
ENST00000479730.5:n.730G=
ENST00000483041.5:n.783G=
ENST00000486063.5:n.794G=
NM_000500.7:c.614G=	NP_000491.4:p.Trp205=
NM_001128590.3:c.524G=	NP_001122062.3:p.Trp175=
XM_011514314.1:c.209G=	XP_011512616.1:p.Trp70=
NM_000500.9:c.614G= MANE Select	NP_000491.4:p.Trp205=
NM_001368143.1:c.209G=	NP_001355072.1:p.Trp70=
NM_001368144.1:c.209G=	NP_001355073.1:p.Trp70=
NM_001128590.4:c.524G=	NP_001122062.3:p.Trp175=
NM_001368143.2:c.209G=	NP_001355072.1:p.Trp70=
NM_001368144.2:c.209G=	NP_001355073.1:p.Trp70=