Canonical Allele Identifier: CA1619396451

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038621C= , CM000668.2:g.32038621C=	GRCh38
NC_000006.11:g.32006398C= , CM000668.1:g.32006398C=	GRCh37
NC_000006.10:g.32114377C=	NCBI36
NG_007941.2:g.5314C=
NG_007941.3:g.5317C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.199C= MANE Select	ENSP00000496625.1:p.Gln67=
ENST00000418967.6:c.199C=	ENSP00000408860.2:p.Gln67=
ENST00000435122.3:c.199C=	ENSP00000415043.2:p.Gln67=
ENST00000464325.5:n.39C=
ENST00000466779.5:c.199C=	ENSP00000417321.1:p.Gln67=
ENST00000469053.5:c.199C=	ENSP00000418104.1:p.Gln67=
ENST00000471671.4:c.199C=	ENSP00000418561.1:p.Gln67=
ENST00000478281.5:c.199C=	ENSP00000419572.1:p.Gln67=
ENST00000479074.5:n.257C=
ENST00000479730.5:n.257C=
ENST00000480027.1:n.252C=
ENST00000483041.5:n.252C=
ENST00000486063.5:n.282C=
ENST00000488465.1:n.207C=
NM_000500.7:c.199C=	NP_000491.4:p.Gln67=
NM_001128590.3:c.199C=	NP_001122062.3:p.Gln67=
XM_011514314.1:c.-226C=	XP_011512616.1:n.-226C=
NM_000500.9:c.199C= MANE Select	NP_000491.4:p.Gln67=
NM_001368143.1:c.-226C=	NP_001355072.1:n.-226C=
NM_001368144.1:c.-136C=	NP_001355073.1:n.-136C=
NM_001128590.4:c.199C=	NP_001122062.3:p.Gln67=
NM_001368143.2:c.-226C=	NP_001355072.1:n.-226C=
NM_001368144.2:c.-136C=	NP_001355073.1:n.-136C=