Canonical Allele Identifier: CA1619396925

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039371C= , CM000668.2:g.32039371C=	GRCh38
NC_000006.11:g.32007148C= , CM000668.1:g.32007148C=	GRCh37
NC_000006.10:g.32115127C=	NCBI36
NG_007941.2:g.6064C=
NG_008337.2:g.75004G=
NG_007941.3:g.6067C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.463C= MANE Select	ENSP00000496625.1:p.Pro155=
ENST00000418967.6:c.463C=	ENSP00000408860.2:p.Pro155=
ENST00000435122.3:c.373C=	ENSP00000415043.2:p.Pro125=
ENST00000462278.1:n.51C=
ENST00000464325.5:n.384C=
ENST00000466779.5:c.*155C=	ENSP00000417321.1:n.*155C=
ENST00000466879.5:n.514C=
ENST00000469053.5:c.*155C=	ENSP00000418104.1:n.*155C=
ENST00000471671.4:c.463C=	ENSP00000418561.1:p.Pro155=
ENST00000478281.5:c.496C=	ENSP00000419572.1:p.Pro166=
ENST00000479074.5:n.521C=
ENST00000479730.5:n.618C=
ENST00000483041.5:n.632C=
ENST00000486063.5:n.643C=
ENST00000488465.1:n.471C=
NM_000500.7:c.463C=	NP_000491.4:p.Pro155=
NM_001128590.3:c.373C=	NP_001122062.3:p.Pro125=
XM_011514314.1:c.58C=	XP_011512616.1:p.Pro20=
NM_000500.9:c.463C= MANE Select	NP_000491.4:p.Pro155=
NM_001368143.1:c.58C=	NP_001355072.1:p.Pro20=
NM_001368144.1:c.58C=	NP_001355073.1:p.Pro20=
NM_001128590.4:c.373C=	NP_001122062.3:p.Pro125=
NM_001368143.2:c.58C=	NP_001355072.1:p.Pro20=
NM_001368144.2:c.58C=	NP_001355073.1:p.Pro20=