Canonical Allele Identifier: CA1619397352

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040187T= , CM000668.2:g.32040187T=	GRCh38
NC_000006.11:g.32007964T= , CM000668.1:g.32007964T=	GRCh37
NC_000006.10:g.32115943T=	NCBI36
NG_007941.2:g.6880T=
NG_008337.2:g.74188A=
NG_007941.3:g.6883T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.921T= MANE Select	ENSP00000496625.1:p.Phe307=
ENST00000418967.6:c.921T=	ENSP00000408860.2:p.Phe307=
ENST00000435122.3:c.831T=	ENSP00000415043.2:p.Phe277=
ENST00000479074.5:n.979T=
ENST00000479730.5:n.1037T=
ENST00000483041.5:n.1090T=
ENST00000486063.5:n.919-219T=
NM_000500.7:c.921T=	NP_000491.4:p.Phe307=
NM_001128590.3:c.831T=	NP_001122062.3:p.Phe277=
XM_011514314.1:c.516T=	XP_011512616.1:p.Phe172=
NM_000500.9:c.921T= MANE Select	NP_000491.4:p.Phe307=
NM_001368143.1:c.516T=	NP_001355072.1:p.Phe172=
NM_001368144.1:c.516T=	NP_001355073.1:p.Phe172=
NM_001128590.4:c.831T=	NP_001122062.3:p.Phe277=
NM_001368143.2:c.516T=	NP_001355072.1:p.Phe172=
NM_001368144.2:c.516T=	NP_001355073.1:p.Phe172=