Canonical Allele Identifier: CA1619396759

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039081C= , CM000668.2:g.32039081C=	GRCh38
NC_000006.11:g.32006858C= , CM000668.1:g.32006858C=	GRCh37
NC_000006.10:g.32114837C=	NCBI36
NG_007941.2:g.5774C=
NG_007941.3:g.5777C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.293-13C= MANE Select	ENSP00000496625.1:n.293-13C=
ENST00000418967.6:c.293-13C=	ENSP00000408860.2:n.293-13C=
ENST00000435122.3:c.203-13C=	ENSP00000415043.2:n.203-13C=
ENST00000464325.5:n.230-29C=
ENST00000466779.5:c.299C=	ENSP00000417321.1:p.Thr100=
ENST00000466879.5:n.331C=
ENST00000469053.5:c.209C=	ENSP00000418104.1:p.Thr70=
ENST00000471671.4:c.293-13C=	ENSP00000418561.1:n.293-13C=
ENST00000478281.5:c.313C=	ENSP00000419572.1:p.Pro105=
ENST00000479074.5:n.351-13C=
ENST00000479730.5:n.448-13C=
ENST00000480027.1:n.615C=
ENST00000483041.5:n.449C=
ENST00000486063.5:n.473-13C=
ENST00000488465.1:n.301-13C=
NM_000500.7:c.293-13C=	NP_000491.4:n.293-13C=
NM_001128590.3:c.203-13C=	NP_001122062.3:n.203-13C=
XM_011514314.1:c.-126C=	XP_011512616.1:n.-126C=
NM_000500.9:c.293-13C= MANE Select	NP_000491.4:n.293-13C=
NM_001368143.1:c.-126C=	NP_001355072.1:n.-126C=
NM_001368144.1:c.-126C=	NP_001355073.1:n.-126C=
NM_001128590.4:c.203-13C=	NP_001122062.3:n.203-13C=
NM_001368143.2:c.-126C=	NP_001355072.1:n.-126C=
NM_001368144.2:c.-126C=	NP_001355073.1:n.-126C=