Canonical Allele Identifier: CA449729103

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007025G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039248G>A , CM000668.2:g.32039248G>A	GRCh38
NC_000006.11:g.32007025G>A , CM000668.1:g.32007025G>A	GRCh37
NC_000006.10:g.32115004G>A	NCBI36
NG_007941.2:g.5941G>A
NG_008337.2:g.75127C>T
NG_007941.3:g.5944G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.447G>A MANE Select	ENSP00000496625.1:p.Glu149=
ENST00000418967.6:c.447G>A	ENSP00000408860.2:p.Glu149=
ENST00000435122.3:c.357G>A	ENSP00000415043.2:p.Glu119=
ENST00000462278.1:n.35G>A
ENST00000464325.5:n.368G>A
ENST00000466779.5:c.*139G>A	ENSP00000417321.1:n.*139G>A
ENST00000466879.5:n.498G>A
ENST00000469053.5:c.*139G>A	ENSP00000418104.1:n.*139G>A
ENST00000471671.4:c.447G>A	ENSP00000418561.1:p.Glu149=
ENST00000478281.5:c.480G>A	ENSP00000419572.1:p.Glu160=
ENST00000479074.5:n.505G>A
ENST00000479730.5:n.602G>A
ENST00000483041.5:n.616G>A
ENST00000486063.5:n.627G>A
ENST00000488465.1:n.455G>A
NM_000500.7:c.447G>A	NP_000491.4:p.Glu149=
NM_001128590.3:c.357G>A	NP_001122062.3:p.Glu119=
XM_011514314.1:c.42G>A	XP_011512616.1:p.Glu14=
NM_000500.9:c.447G>A MANE Select	NP_000491.4:p.Glu149=
NM_001368143.1:c.42G>A	NP_001355072.1:p.Glu14=
NM_001368144.1:c.42G>A	NP_001355073.1:p.Glu14=
NM_001128590.4:c.357G>A	NP_001122062.3:p.Glu119=
NM_001368143.2:c.42G>A	NP_001355072.1:p.Glu14=
NM_001368144.2:c.42G>A	NP_001355073.1:p.Glu14=