Canonical Allele Identifier: CA1619397468

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040433G= , CM000668.2:g.32040433G=	GRCh38
NC_000006.11:g.32008210G= , CM000668.1:g.32008210G=	GRCh37
NC_000006.10:g.32116189G=	NCBI36
NG_007941.2:g.7126G=
NG_008337.2:g.73942C=
NG_007941.3:g.7129G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.967G= MANE Select	ENSP00000496625.1:p.Asp323=
ENST00000418967.6:c.967G=	ENSP00000408860.2:p.Asp323=
ENST00000435122.3:c.877G=	ENSP00000415043.2:p.Asp293=
ENST00000479074.5:n.1025G=
ENST00000479730.5:n.1083G=
ENST00000483041.5:n.1136G=
ENST00000486063.5:n.946G=
NM_000500.7:c.967G=	NP_000491.4:p.Asp323=
NM_001128590.3:c.877G=	NP_001122062.3:p.Asp293=
XM_011514314.1:c.562G=	XP_011512616.1:p.Asp188=
NM_000500.9:c.967G= MANE Select	NP_000491.4:p.Asp323=
NM_001368143.1:c.562G=	NP_001355072.1:p.Asp188=
NM_001368144.1:c.562G=	NP_001355073.1:p.Asp188=
NM_001128590.4:c.877G=	NP_001122062.3:p.Asp293=
NM_001368143.2:c.562G=	NP_001355072.1:p.Asp188=
NM_001368144.2:c.562G=	NP_001355073.1:p.Asp188=