Canonical Allele Identifier: CA1619399240

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040471C= , CM000668.2:g.32040471C=	GRCh38
NC_000006.11:g.32008248C= , CM000668.1:g.32008248C=	GRCh37
NC_000006.10:g.32116227C=	NCBI36
NG_007941.2:g.7164C=
NG_008337.2:g.73904G=
NG_007941.3:g.7167C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1005C= MANE Select	ENSP00000496625.1:p.Val335=
ENST00000418967.6:c.1005C=	ENSP00000408860.2:p.Val335=
ENST00000435122.3:c.915C=	ENSP00000415043.2:p.Val305=
ENST00000479074.5:n.1063C=
ENST00000479730.5:n.1121C=
ENST00000483041.5:n.1174C=
ENST00000486063.5:n.984C=
NM_000500.7:c.1005C=	NP_000491.4:p.Val335=
NM_001128590.3:c.915C=	NP_001122062.3:p.Val305=
XM_011514314.1:c.600C=	XP_011512616.1:p.Val200=
NM_000500.9:c.1005C= MANE Select	NP_000491.4:p.Val335=
NM_001368143.1:c.600C=	NP_001355072.1:p.Val200=
NM_001368144.1:c.600C=	NP_001355073.1:p.Val200=
NM_001128590.4:c.915C=	NP_001122062.3:p.Val305=
NM_001368143.2:c.600C=	NP_001355072.1:p.Val200=
NM_001368144.2:c.600C=	NP_001355073.1:p.Val200=