Canonical Allele Identifier: CA1619397253

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039969G= , CM000668.2:g.32039969G=	GRCh38
NC_000006.11:g.32007746G= , CM000668.1:g.32007746G=	GRCh37
NC_000006.10:g.32115725G=	NCBI36
NG_007941.2:g.6662G=
NG_008337.2:g.74406C=
NG_007941.3:g.6665G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.739-36G= MANE Select	ENSP00000496625.1:n.739-36G=
ENST00000418967.6:c.739-36G=	ENSP00000408860.2:n.739-36G=
ENST00000435122.3:c.649-36G=	ENSP00000415043.2:n.649-36G=
ENST00000462278.1:n.561G=
ENST00000479074.5:n.797-36G=
ENST00000479730.5:n.855-36G=
ENST00000483041.5:n.908-36G=
ENST00000486063.5:n.918+134G=
NM_000500.7:c.739-36G=	NP_000491.4:n.739-36G=
NM_001128590.3:c.649-36G=	NP_001122062.3:n.649-36G=
XM_011514314.1:c.334-36G=	XP_011512616.1:n.334-36G=
NM_000500.9:c.739-36G= MANE Select	NP_000491.4:n.739-36G=
NM_001368143.1:c.334-36G=	NP_001355072.1:n.334-36G=
NM_001368144.1:c.334-36G=	NP_001355073.1:n.334-36G=
NM_001128590.4:c.649-36G=	NP_001122062.3:n.649-36G=
NM_001368143.2:c.334-36G=	NP_001355072.1:n.334-36G=
NM_001368144.2:c.334-36G=	NP_001355073.1:n.334-36G=