Canonical Allele Identifier: CA1619397055

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039585G= , CM000668.2:g.32039585G=	GRCh38
NC_000006.11:g.32007362G= , CM000668.1:g.32007362G=	GRCh37
NC_000006.10:g.32115341G=	NCBI36
NG_007941.2:g.6278G=
NG_008337.2:g.74790C=
NG_007941.3:g.6281G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.589G= MANE Select	ENSP00000496625.1:p.Glu197=
ENST00000418967.6:c.589G=	ENSP00000408860.2:p.Glu197=
ENST00000435122.3:c.499G=	ENSP00000415043.2:p.Glu167=
ENST00000462278.1:n.177G=
ENST00000464325.5:n.510G=
ENST00000466779.5:c.*281G=	ENSP00000417321.1:n.*281G=
ENST00000466879.5:n.640G=
ENST00000469053.5:c.*281G=	ENSP00000418104.1:n.*281G=
ENST00000471671.4:c.550G=	ENSP00000418561.1:p.Glu184=
ENST00000479074.5:n.647G=
ENST00000479730.5:n.705G=
ENST00000483041.5:n.758G=
ENST00000486063.5:n.769G=
NM_000500.7:c.589G=	NP_000491.4:p.Glu197=
NM_001128590.3:c.499G=	NP_001122062.3:p.Glu167=
XM_011514314.1:c.184G=	XP_011512616.1:p.Glu62=
NM_000500.9:c.589G= MANE Select	NP_000491.4:p.Glu197=
NM_001368143.1:c.184G=	NP_001355072.1:p.Glu62=
NM_001368144.1:c.184G=	NP_001355073.1:p.Glu62=
NM_001128590.4:c.499G=	NP_001122062.3:p.Glu167=
NM_001368143.2:c.184G=	NP_001355072.1:p.Glu62=
NM_001368144.2:c.184G=	NP_001355073.1:p.Glu62=