Canonical Allele Identifier: CA1619396777

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039106C= , CM000668.2:g.32039106C=	GRCh38
NC_000006.11:g.32006883C= , CM000668.1:g.32006883C=	GRCh37
NC_000006.10:g.32114862C=	NCBI36
NG_007941.2:g.5799C=
NG_007941.3:g.5802C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.305C= MANE Select	ENSP00000496625.1:p.Ser102=
ENST00000418967.6:c.305C=	ENSP00000408860.2:p.Ser102=
ENST00000435122.3:c.215C=	ENSP00000415043.2:p.Ser72=
ENST00000464325.5:n.230-4C=
ENST00000466779.5:c.324C=	ENSP00000417321.1:p.Val108=
ENST00000466879.5:n.356C=
ENST00000469053.5:c.234C=	ENSP00000418104.1:p.Val78=
ENST00000471671.4:c.305C=	ENSP00000418561.1:p.Ser102=
ENST00000478281.5:c.338C=	ENSP00000419572.1:p.Ser113=
ENST00000479074.5:n.363C=
ENST00000479730.5:n.460C=
ENST00000480027.1:n.640C=
ENST00000483041.5:n.474C=
ENST00000486063.5:n.485C=
ENST00000488465.1:n.313C=
NM_000500.7:c.305C=	NP_000491.4:p.Ser102=
NM_001128590.3:c.215C=	NP_001122062.3:p.Ser72=
XM_011514314.1:c.-101C=	XP_011512616.1:n.-101C=
NM_000500.9:c.305C= MANE Select	NP_000491.4:p.Ser102=
NM_001368143.1:c.-101C=	NP_001355072.1:n.-101C=
NM_001368144.1:c.-101C=	NP_001355073.1:n.-101C=
NM_001128590.4:c.215C=	NP_001122062.3:p.Ser72=
NM_001368143.2:c.-101C=	NP_001355072.1:n.-101C=
NM_001368144.2:c.-101C=	NP_001355073.1:n.-101C=