Canonical Allele Identifier: CA1619396823

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039195A= , CM000668.2:g.32039195A=	GRCh38
NC_000006.11:g.32006972A= , CM000668.1:g.32006972A=	GRCh37
NC_000006.10:g.32114951A=	NCBI36
NG_007941.2:g.5888A=
NG_008337.2:g.75180T=
NG_007941.3:g.5891A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.394A= MANE Select	ENSP00000496625.1:p.Ile132=
ENST00000418967.6:c.394A=	ENSP00000408860.2:p.Ile132=
ENST00000435122.3:c.304A=	ENSP00000415043.2:p.Ile102=
ENST00000464325.5:n.315A=
ENST00000466779.5:c.*86A=	ENSP00000417321.1:n.*86A=
ENST00000466879.5:n.445A=
ENST00000469053.5:c.*86A=	ENSP00000418104.1:n.*86A=
ENST00000471671.4:c.394A=	ENSP00000418561.1:p.Ile132=
ENST00000478281.5:c.427A=	ENSP00000419572.1:p.Ile143=
ENST00000479074.5:n.452A=
ENST00000479730.5:n.549A=
ENST00000483041.5:n.563A=
ENST00000486063.5:n.574A=
ENST00000488465.1:n.402A=
NM_000500.7:c.394A=	NP_000491.4:p.Ile132=
NM_001128590.3:c.304A=	NP_001122062.3:p.Ile102=
XM_011514314.1:c.-12A=	XP_011512616.1:n.-12A=
NM_000500.9:c.394A= MANE Select	NP_000491.4:p.Ile132=
NM_001368143.1:c.-12A=	NP_001355072.1:n.-12A=
NM_001368144.1:c.-12A=	NP_001355073.1:n.-12A=
NM_001128590.4:c.304A=	NP_001122062.3:p.Ile102=
NM_001368143.2:c.-12A=	NP_001355072.1:n.-12A=
NM_001368144.2:c.-12A=	NP_001355073.1:n.-12A=