Canonical Allele Identifier: CA1619396930

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039385G= , CM000668.2:g.32039385G=	GRCh38
NC_000006.11:g.32007162G= , CM000668.1:g.32007162G=	GRCh37
NC_000006.10:g.32115141G=	NCBI36
NG_007941.2:g.6078G=
NG_008337.2:g.74990C=
NG_007941.3:g.6081G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.477G= MANE Select	ENSP00000496625.1:p.Val159=
ENST00000418967.6:c.477G=	ENSP00000408860.2:p.Val159=
ENST00000435122.3:c.387G=	ENSP00000415043.2:p.Val129=
ENST00000462278.1:n.65G=
ENST00000464325.5:n.398G=
ENST00000466779.5:c.*169G=	ENSP00000417321.1:n.*169G=
ENST00000466879.5:n.528G=
ENST00000469053.5:c.*169G=	ENSP00000418104.1:n.*169G=
ENST00000471671.4:c.477G=	ENSP00000418561.1:p.Val159=
ENST00000478281.5:c.510G=	ENSP00000419572.1:p.Val170=
ENST00000479074.5:n.535G=
ENST00000479730.5:n.632G=
ENST00000483041.5:n.646G=
ENST00000486063.5:n.657G=
ENST00000488465.1:n.485G=
NM_000500.7:c.477G=	NP_000491.4:p.Val159=
NM_001128590.3:c.387G=	NP_001122062.3:p.Val129=
XM_011514314.1:c.72G=	XP_011512616.1:p.Val24=
NM_000500.9:c.477G= MANE Select	NP_000491.4:p.Val159=
NM_001368143.1:c.72G=	NP_001355072.1:p.Val24=
NM_001368144.1:c.72G=	NP_001355073.1:p.Val24=
NM_001128590.4:c.387G=	NP_001122062.3:p.Val129=
NM_001368143.2:c.72G=	NP_001355072.1:p.Val24=
NM_001368144.2:c.72G=	NP_001355073.1:p.Val24=