Canonical Allele Identifier: CA1619396477

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038681A= , CM000668.2:g.32038681A=	GRCh38
NC_000006.11:g.32006458A= , CM000668.1:g.32006458A=	GRCh37
NC_000006.10:g.32114437A=	NCBI36
NG_007941.2:g.5374A=
NG_007941.3:g.5377A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.203-41A= MANE Select	ENSP00000496625.1:n.203-41A=
ENST00000418967.6:c.203-41A=	ENSP00000408860.2:n.203-41A=
ENST00000435122.3:c.202+57A=	ENSP00000415043.2:n.202+57A=
ENST00000464325.5:n.99A=
ENST00000466779.5:c.203-41A=	ENSP00000417321.1:n.203-41A=
ENST00000469053.5:c.202+57A=	ENSP00000418104.1:n.202+57A=
ENST00000471671.4:c.203-41A=	ENSP00000418561.1:n.203-41A=
ENST00000478281.5:c.203-41A=	ENSP00000419572.1:n.203-41A=
ENST00000479074.5:n.261-41A=
ENST00000479730.5:n.317A=
ENST00000480027.1:n.256-41A=
ENST00000483041.5:n.312A=
ENST00000486063.5:n.342A=
ENST00000488465.1:n.211-41A=
NM_000500.7:c.203-41A=	NP_000491.4:n.203-41A=
NM_001128590.3:c.202+57A=	NP_001122062.3:n.202+57A=
XM_011514314.1:c.-222-41A=	XP_011512616.1:n.-222-41A=
NM_000500.9:c.203-41A= MANE Select	NP_000491.4:n.203-41A=
NM_001368143.1:c.-222-41A=	NP_001355072.1:n.-222-41A=
NM_001368144.1:c.-133+57A=	NP_001355073.1:n.-133+57A=
NM_001128590.4:c.202+57A=	NP_001122062.3:n.202+57A=
NM_001368143.2:c.-222-41A=	NP_001355072.1:n.-222-41A=
NM_001368144.2:c.-133+57A=	NP_001355073.1:n.-133+57A=