Canonical Allele Identifier: CA1619397347

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040179G= , CM000668.2:g.32040179G=	GRCh38
NC_000006.11:g.32007956G= , CM000668.1:g.32007956G=	GRCh37
NC_000006.10:g.32115935G=	NCBI36
NG_007941.2:g.6872G=
NG_008337.2:g.74196C=
NG_007941.3:g.6875G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000500.9:c.913G= MANE Select	NP_000491.4:p.Val305=
ENST00000644719.2:c.913G= MANE Select	ENSP00000496625.1:p.Val305=
NM_000500.7:c.913G=	NP_000491.4:p.Val305=
NM_001128590.3:c.823G=	NP_001122062.3:p.Val275=
NM_001128590.4:c.823G=	NP_001122062.3:p.Val275=
NM_001368143.1:c.508G=	NP_001355072.1:p.Val170=
NM_001368143.2:c.508G=	NP_001355072.1:p.Val170=
NM_001368144.1:c.508G=	NP_001355073.1:p.Val170=
NM_001368144.2:c.508G=	NP_001355073.1:p.Val170=
ENST00000418967.6:c.913G=	ENSP00000408860.2:p.Val305=
ENST00000435122.3:c.823G=	ENSP00000415043.2:p.Val275=
ENST00000479074.5:n.971G=
ENST00000479730.5:n.1029G=
ENST00000483041.5:n.1082G=
ENST00000486063.5:n.919-227G=
XM_011514314.1:c.508G=	XP_011512616.1:p.Val170=