Canonical Allele Identifier: CA1619396838

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039221G= , CM000668.2:g.32039221G=	GRCh38
NC_000006.11:g.32006998G= , CM000668.1:g.32006998G=	GRCh37
NC_000006.10:g.32114977G=	NCBI36
NG_007941.2:g.5914G=
NG_008337.2:g.75154C=
NG_007941.3:g.5917G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.420G= MANE Select	ENSP00000496625.1:p.Val140=
ENST00000418967.6:c.420G=	ENSP00000408860.2:p.Val140=
ENST00000435122.3:c.330G=	ENSP00000415043.2:p.Val110=
ENST00000462278.1:n.8G=
ENST00000464325.5:n.341G=
ENST00000466779.5:c.*112G=	ENSP00000417321.1:n.*112G=
ENST00000466879.5:n.471G=
ENST00000469053.5:c.*112G=	ENSP00000418104.1:n.*112G=
ENST00000471671.4:c.420G=	ENSP00000418561.1:p.Val140=
ENST00000478281.5:c.453G=	ENSP00000419572.1:p.Val151=
ENST00000479074.5:n.478G=
ENST00000479730.5:n.575G=
ENST00000483041.5:n.589G=
ENST00000486063.5:n.600G=
ENST00000488465.1:n.428G=
NM_000500.7:c.420G=	NP_000491.4:p.Val140=
NM_001128590.3:c.330G=	NP_001122062.3:p.Val110=
XM_011514314.1:c.15G=	XP_011512616.1:p.Val5=
NM_000500.9:c.420G= MANE Select	NP_000491.4:p.Val140=
NM_001368143.1:c.15G=	NP_001355072.1:p.Val5=
NM_001368144.1:c.15G=	NP_001355073.1:p.Val5=
NM_001128590.4:c.330G=	NP_001122062.3:p.Val110=
NM_001368143.2:c.15G=	NP_001355072.1:p.Val5=
NM_001368144.2:c.15G=	NP_001355073.1:p.Val5=