Canonical Allele Identifier: CA1619397217

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039888C= , CM000668.2:g.32039888C=	GRCh38
NC_000006.11:g.32007665C= , CM000668.1:g.32007665C=	GRCh37
NC_000006.10:g.32115644C=	NCBI36
NG_007941.2:g.6581C=
NG_008337.2:g.74487G=
NG_007941.3:g.6584C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.738+53C= MANE Select	ENSP00000496625.1:n.738+53C=
ENST00000418967.6:c.738+53C=	ENSP00000408860.2:n.738+53C=
ENST00000435122.3:c.648+53C=	ENSP00000415043.2:n.648+53C=
ENST00000462278.1:n.480C=
ENST00000479074.5:n.796+53C=
ENST00000479730.5:n.854+53C=
ENST00000483041.5:n.907+53C=
ENST00000486063.5:n.918+53C=
NM_000500.7:c.738+53C=	NP_000491.4:n.738+53C=
NM_001128590.3:c.648+53C=	NP_001122062.3:n.648+53C=
XM_011514314.1:c.333+53C=	XP_011512616.1:n.333+53C=
NM_000500.9:c.738+53C= MANE Select	NP_000491.4:n.738+53C=
NM_001368143.1:c.333+53C=	NP_001355072.1:n.333+53C=
NM_001368144.1:c.333+53C=	NP_001355073.1:n.333+53C=
NM_001128590.4:c.648+53C=	NP_001122062.3:n.648+53C=
NM_001368143.2:c.333+53C=	NP_001355072.1:n.333+53C=
NM_001368144.2:c.333+53C=	NP_001355073.1:n.333+53C=