Canonical Allele Identifier: CA1619396338

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038420G= , CM000668.2:g.32038420G=	GRCh38
NC_000006.11:g.32006197G= , CM000668.1:g.32006197G=	GRCh37
NC_000006.10:g.32114176G=	NCBI36
NG_007941.2:g.5116G=
NG_007941.3:g.5116G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.-3G= MANE Select	ENSP00000496625.1:n.-3G=
ENST00000418967.6:c.-3G=	ENSP00000408860.2:n.-3G=
ENST00000435122.3:c.-3G=	ENSP00000415043.2:n.-3G=
ENST00000466779.5:c.-3G=	ENSP00000417321.1:n.-3G=
ENST00000469053.5:c.-3G=	ENSP00000418104.1:n.-3G=
ENST00000471671.4:c.-3G=	ENSP00000418561.1:n.-3G=
ENST00000478281.5:c.-3G=	ENSP00000419572.1:n.-3G=
ENST00000479074.5:n.56G=
ENST00000479730.5:n.56G=
ENST00000480027.1:n.51G=
ENST00000483041.5:n.51G=
ENST00000486063.5:n.81G=
ENST00000488465.1:n.6G=
NM_000500.7:c.-3G=	NP_000491.4:n.-3G=
NM_001128590.3:c.-3G=	NP_001122062.3:n.-3G=
XM_011514314.1:c.-427G=	XP_011512616.1:n.-427G=
NM_000500.9:c.-3G= MANE Select	NP_000491.4:n.-3G=
NM_001368143.1:c.-427G=	NP_001355072.1:n.-427G=
NM_001368144.1:c.-337G=	NP_001355073.1:n.-337G=
NM_001128590.4:c.-3G=	NP_001122062.3:n.-3G=
NM_001368143.2:c.-427G=	NP_001355072.1:n.-427G=
NM_001368144.2:c.-337G=	NP_001355073.1:n.-337G=