Canonical Allele Identifier: CA1619397336

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040152A= , CM000668.2:g.32040152A=	GRCh38
NC_000006.11:g.32007929A= , CM000668.1:g.32007929A=	GRCh37
NC_000006.10:g.32115908A=	NCBI36
NG_007941.2:g.6845A=
NG_008337.2:g.74223T=
NG_007941.3:g.6848A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.886A= MANE Select	ENSP00000496625.1:p.Thr296=
ENST00000418967.6:c.886A=	ENSP00000408860.2:p.Thr296=
ENST00000435122.3:c.796A=	ENSP00000415043.2:p.Thr266=
ENST00000479074.5:n.944A=
ENST00000479730.5:n.1002A=
ENST00000483041.5:n.1055A=
ENST00000486063.5:n.919-254A=
NM_000500.7:c.886A=	NP_000491.4:p.Thr296=
NM_001128590.3:c.796A=	NP_001122062.3:p.Thr266=
XM_011514314.1:c.481A=	XP_011512616.1:p.Thr161=
NM_000500.9:c.886A= MANE Select	NP_000491.4:p.Thr296=
NM_001368143.1:c.481A=	NP_001355072.1:p.Thr161=
NM_001368144.1:c.481A=	NP_001355073.1:p.Thr161=
NM_001128590.4:c.796A=	NP_001122062.3:p.Thr266=
NM_001368143.2:c.481A=	NP_001355072.1:p.Thr161=
NM_001368144.2:c.481A=	NP_001355073.1:p.Thr161=