Canonical Allele Identifier: CA1619397432

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040357T= , CM000668.2:g.32040357T=	GRCh38
NC_000006.11:g.32008134T= , CM000668.1:g.32008134T=	GRCh37
NC_000006.10:g.32116113T=	NCBI36
NG_007941.2:g.7050T=
NG_008337.2:g.74018A=
NG_007941.3:g.7053T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.940-49T= MANE Select	ENSP00000496625.1:n.940-49T=
ENST00000418967.6:c.940-49T=	ENSP00000408860.2:n.940-49T=
ENST00000435122.3:c.850-49T=	ENSP00000415043.2:n.850-49T=
ENST00000479074.5:n.998-49T=
ENST00000479730.5:n.1056-49T=
ENST00000483041.5:n.1109-49T=
ENST00000486063.5:n.919-49T=
NM_000500.7:c.940-49T=	NP_000491.4:n.940-49T=
NM_001128590.3:c.850-49T=	NP_001122062.3:n.850-49T=
XM_011514314.1:c.535-49T=	XP_011512616.1:n.535-49T=
NM_000500.9:c.940-49T= MANE Select	NP_000491.4:n.940-49T=
NM_001368143.1:c.535-49T=	NP_001355072.1:n.535-49T=
NM_001368144.1:c.535-49T=	NP_001355073.1:n.535-49T=
NM_001128590.4:c.850-49T=	NP_001122062.3:n.850-49T=
NM_001368143.2:c.535-49T=	NP_001355072.1:n.535-49T=
NM_001368144.2:c.535-49T=	NP_001355073.1:n.535-49T=