Canonical Allele Identifier: CA1619396346

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038435_32038438delinsGGCC , CM000668.2:g.32038435_32038438delinsGGCC	GRCh38
NC_000006.11:g.32006212_32006215delinsGGCC , CM000668.1:g.32006212_32006215delinsGGCC	GRCh37
NC_000006.10:g.32114191_32114194delinsGGCC	NCBI36
NG_007941.3:g.5131_5134delinsGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.13_16delinsGGCC MANE Select	ENSP00000496625.1:p.Gly5=
ENST00000418967.6:c.13_16delinsGGCC	ENSP00000408860.2:p.Gly5=
ENST00000435122.3:c.13_16delinsGGCC	ENSP00000415043.2:p.Gly5=
ENST00000466779.5:c.13_16delinsGGCC	ENSP00000417321.1:p.Gly5=
ENST00000469053.5:c.13_16delinsGGCC	ENSP00000418104.1:p.Gly5=
ENST00000471671.4:c.13_16delinsGGCC	ENSP00000418561.1:p.Gly5=
ENST00000478281.5:c.13_16delinsGGCC	ENSP00000419572.1:p.Gly5=
ENST00000479074.5:n.71_74delinsGGCC
ENST00000479730.5:n.71_74delinsGGCC
ENST00000480027.1:n.66_69delinsGGCC
ENST00000483041.5:n.66_69delinsGGCC
ENST00000486063.5:n.96_99delinsGGCC
ENST00000488465.1:n.21_24delinsGGCC
NM_000500.7:c.13_16delinsGGCC	NP_000491.4:p.Gly5=
NM_001128590.3:c.13_16delinsGGCC	NP_001122062.3:p.Gly5=
XM_011514314.1:c.-412_-409delinsGGCC	XP_011512616.1:n.-412_-409delinsGGCC
NM_000500.9:c.13_16delinsGGCC MANE Select	NP_000491.4:p.Gly5=
NM_001368143.1:c.-412_-409delinsGGCC	NP_001355072.1:n.-412_-409delinsGGCC
NM_001368144.1:c.-322_-319delinsGGCC	NP_001355073.1:n.-322_-319delinsGGCC
NM_001128590.4:c.13_16delinsGGCC	NP_001122062.3:p.Gly5=
NM_001368143.2:c.-412_-409delinsGGCC	NP_001355072.1:n.-412_-409delinsGGCC
NM_001368144.2:c.-322_-319delinsGGCC	NP_001355073.1:n.-322_-319delinsGGCC