Canonical Allele Identifier: CA1619396646

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038958C= , CM000668.2:g.32038958C=	GRCh38
NC_000006.11:g.32006735C= , CM000668.1:g.32006735C=	GRCh37
NC_000006.10:g.32114714C=	NCBI36
NG_007941.2:g.5651C=
NG_007941.3:g.5654C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.293-136C= MANE Select	ENSP00000496625.1:n.293-136C=
ENST00000418967.6:c.293-136C=	ENSP00000408860.2:n.293-136C=
ENST00000435122.3:c.203-136C=	ENSP00000415043.2:n.203-136C=
ENST00000464325.5:n.229+147C=
ENST00000466779.5:c.293-117C=	ENSP00000417321.1:n.293-117C=
ENST00000466879.5:n.208C=
ENST00000469053.5:c.203-117C=	ENSP00000418104.1:n.203-117C=
ENST00000471671.4:c.293-136C=	ENSP00000418561.1:n.293-136C=
ENST00000478281.5:c.293-103C=	ENSP00000419572.1:n.293-103C=
ENST00000479074.5:n.351-136C=
ENST00000479730.5:n.448-136C=
ENST00000480027.1:n.492C=
ENST00000483041.5:n.443-117C=
ENST00000486063.5:n.473-136C=
ENST00000488465.1:n.301-136C=
NM_000500.7:c.293-136C=	NP_000491.4:n.293-136C=
NM_001128590.3:c.203-136C=	NP_001122062.3:n.203-136C=
XM_011514314.1:c.-132-117C=	XP_011512616.1:n.-132-117C=
NM_000500.9:c.293-136C= MANE Select	NP_000491.4:n.293-136C=
NM_001368143.1:c.-132-117C=	NP_001355072.1:n.-132-117C=
NM_001368144.1:c.-132-117C=	NP_001355073.1:n.-132-117C=
NM_001128590.4:c.203-136C=	NP_001122062.3:n.203-136C=
NM_001368143.2:c.-132-117C=	NP_001355072.1:n.-132-117C=
NM_001368144.2:c.-132-117C=	NP_001355073.1:n.-132-117C=