Canonical Allele Identifier: CA1619396923

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039369A= , CM000668.2:g.32039369A=	GRCh38
NC_000006.11:g.32007146A= , CM000668.1:g.32007146A=	GRCh37
NC_000006.10:g.32115125A=	NCBI36
NG_007941.2:g.6062A=
NG_008337.2:g.75006T=
NG_007941.3:g.6065A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.461A= MANE Select	ENSP00000496625.1:p.Gln154=
ENST00000418967.6:c.461A=	ENSP00000408860.2:p.Gln154=
ENST00000435122.3:c.371A=	ENSP00000415043.2:p.Gln124=
ENST00000462278.1:n.49A=
ENST00000464325.5:n.382A=
ENST00000466779.5:c.*153A=	ENSP00000417321.1:n.*153A=
ENST00000466879.5:n.512A=
ENST00000469053.5:c.*153A=	ENSP00000418104.1:n.*153A=
ENST00000471671.4:c.461A=	ENSP00000418561.1:p.Gln154=
ENST00000478281.5:c.494A=	ENSP00000419572.1:p.Gln165=
ENST00000479074.5:n.519A=
ENST00000479730.5:n.616A=
ENST00000483041.5:n.630A=
ENST00000486063.5:n.641A=
ENST00000488465.1:n.469A=
NM_000500.7:c.461A=	NP_000491.4:p.Gln154=
NM_001128590.3:c.371A=	NP_001122062.3:p.Gln124=
XM_011514314.1:c.56A=	XP_011512616.1:p.Gln19=
NM_000500.9:c.461A= MANE Select	NP_000491.4:p.Gln154=
NM_001368143.1:c.56A=	NP_001355072.1:p.Gln19=
NM_001368144.1:c.56A=	NP_001355073.1:p.Gln19=
NM_001128590.4:c.371A=	NP_001122062.3:p.Gln124=
NM_001368143.2:c.56A=	NP_001355072.1:p.Gln19=
NM_001368144.2:c.56A=	NP_001355073.1:p.Gln19=