Canonical Allele Identifier: CA1619397328

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040130C= , CM000668.2:g.32040130C=	GRCh38
NC_000006.11:g.32007907C= , CM000668.1:g.32007907C=	GRCh37
NC_000006.10:g.32115886C=	NCBI36
NG_007941.2:g.6823C=
NG_008337.2:g.74245G=
NG_007941.3:g.6826C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.864C= MANE Select	ENSP00000496625.1:p.Asp288=
ENST00000418967.6:c.864C=	ENSP00000408860.2:p.Asp288=
ENST00000435122.3:c.774C=	ENSP00000415043.2:p.Asp258=
ENST00000479074.5:n.922C=
ENST00000479730.5:n.980C=
ENST00000483041.5:n.1033C=
ENST00000486063.5:n.919-276C=
NM_000500.7:c.864C=	NP_000491.4:p.Asp288=
NM_001128590.3:c.774C=	NP_001122062.3:p.Asp258=
XM_011514314.1:c.459C=	XP_011512616.1:p.Asp153=
NM_000500.9:c.864C= MANE Select	NP_000491.4:p.Asp288=
NM_001368143.1:c.459C=	NP_001355072.1:p.Asp153=
NM_001368144.1:c.459C=	NP_001355073.1:p.Asp153=
NM_001128590.4:c.774C=	NP_001122062.3:p.Asp258=
NM_001368143.2:c.459C=	NP_001355072.1:p.Asp153=
NM_001368144.2:c.459C=	NP_001355073.1:p.Asp153=