Canonical Allele Identifier: CA1619397427

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040346C= , CM000668.2:g.32040346C=	GRCh38
NC_000006.11:g.32008123C= , CM000668.1:g.32008123C=	GRCh37
NC_000006.10:g.32116102C=	NCBI36
NG_007941.2:g.7039C=
NG_008337.2:g.74029G=
NG_007941.3:g.7042C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.940-60C= MANE Select	ENSP00000496625.1:n.940-60C=
ENST00000418967.6:c.940-60C=	ENSP00000408860.2:n.940-60C=
ENST00000435122.3:c.850-60C=	ENSP00000415043.2:n.850-60C=
ENST00000479074.5:n.998-60C=
ENST00000479730.5:n.1056-60C=
ENST00000483041.5:n.1109-60C=
ENST00000486063.5:n.919-60C=
NM_000500.7:c.940-60C=	NP_000491.4:n.940-60C=
NM_001128590.3:c.850-60C=	NP_001122062.3:n.850-60C=
XM_011514314.1:c.535-60C=	XP_011512616.1:n.535-60C=
NM_000500.9:c.940-60C= MANE Select	NP_000491.4:n.940-60C=
NM_001368143.1:c.535-60C=	NP_001355072.1:n.535-60C=
NM_001368144.1:c.535-60C=	NP_001355073.1:n.535-60C=
NM_001128590.4:c.850-60C=	NP_001122062.3:n.850-60C=
NM_001368143.2:c.535-60C=	NP_001355072.1:n.535-60C=
NM_001368144.2:c.535-60C=	NP_001355073.1:n.535-60C=