Canonical Allele Identifier: CA1619397220

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039892C= , CM000668.2:g.32039892C=	GRCh38
NC_000006.11:g.32007669C= , CM000668.1:g.32007669C=	GRCh37
NC_000006.10:g.32115648C=	NCBI36
NG_007941.2:g.6585C=
NG_008337.2:g.74483G=
NG_007941.3:g.6588C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.738+57C= MANE Select	ENSP00000496625.1:n.738+57C=
ENST00000418967.6:c.738+57C=	ENSP00000408860.2:n.738+57C=
ENST00000435122.3:c.648+57C=	ENSP00000415043.2:n.648+57C=
ENST00000462278.1:n.484C=
ENST00000479074.5:n.796+57C=
ENST00000479730.5:n.854+57C=
ENST00000483041.5:n.907+57C=
ENST00000486063.5:n.918+57C=
NM_000500.7:c.738+57C=	NP_000491.4:n.738+57C=
NM_001128590.3:c.648+57C=	NP_001122062.3:n.648+57C=
XM_011514314.1:c.333+57C=	XP_011512616.1:n.333+57C=
NM_000500.9:c.738+57C= MANE Select	NP_000491.4:n.738+57C=
NM_001368143.1:c.333+57C=	NP_001355072.1:n.333+57C=
NM_001368144.1:c.333+57C=	NP_001355073.1:n.333+57C=
NM_001128590.4:c.648+57C=	NP_001122062.3:n.648+57C=
NM_001368143.2:c.333+57C=	NP_001355072.1:n.333+57C=
NM_001368144.2:c.333+57C=	NP_001355073.1:n.333+57C=