Canonical Allele Identifier: CA1619396348

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038437_32038440delinsCCTG , CM000668.2:g.32038437_32038440delinsCCTG	GRCh38
NC_000006.11:g.32006214_32006217delinsCCTG , CM000668.1:g.32006214_32006217delinsCCTG	GRCh37
NC_000006.10:g.32114193_32114196delinsCCTG	NCBI36
NG_007941.3:g.5133_5136delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.15_18delinsCCTG MANE Select	ENSP00000496625.1:p.Gly5=
ENST00000418967.6:c.15_18delinsCCTG	ENSP00000408860.2:p.Gly5=
ENST00000435122.3:c.15_18delinsCCTG	ENSP00000415043.2:p.Gly5=
ENST00000466779.5:c.15_18delinsCCTG	ENSP00000417321.1:p.Gly5=
ENST00000469053.5:c.15_18delinsCCTG	ENSP00000418104.1:p.Gly5=
ENST00000471671.4:c.15_18delinsCCTG	ENSP00000418561.1:p.Gly5=
ENST00000478281.5:c.15_18delinsCCTG	ENSP00000419572.1:p.Gly5=
ENST00000479074.5:n.73_76delinsCCTG
ENST00000479730.5:n.73_76delinsCCTG
ENST00000480027.1:n.68_71delinsCCTG
ENST00000483041.5:n.68_71delinsCCTG
ENST00000486063.5:n.98_101delinsCCTG
ENST00000488465.1:n.23_26delinsCCTG
NM_000500.7:c.15_18delinsCCTG	NP_000491.4:p.Gly5=
NM_001128590.3:c.15_18delinsCCTG	NP_001122062.3:p.Gly5=
XM_011514314.1:c.-410_-407delinsCCTG	XP_011512616.1:n.-410_-407delinsCCTG
NM_000500.9:c.15_18delinsCCTG MANE Select	NP_000491.4:p.Gly5=
NM_001368143.1:c.-410_-407delinsCCTG	NP_001355072.1:n.-410_-407delinsCCTG
NM_001368144.1:c.-320_-317delinsCCTG	NP_001355073.1:n.-320_-317delinsCCTG
NM_001128590.4:c.15_18delinsCCTG	NP_001122062.3:p.Gly5=
NM_001368143.2:c.-410_-407delinsCCTG	NP_001355072.1:n.-410_-407delinsCCTG
NM_001368144.2:c.-320_-317delinsCCTG	NP_001355073.1:n.-320_-317delinsCCTG