Canonical Allele Identifier: CA2578617999

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039266A>G , CM000668.2:g.32039266A>G	GRCh38
NC_000006.11:g.32007043A>G , CM000668.1:g.32007043A>G	GRCh37
NC_000006.10:g.32115022A>G	NCBI36
NG_007941.2:g.5959A>G
NG_008337.2:g.75109T>C
NG_007941.3:g.5962A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.447+18A>G MANE Select	ENSP00000496625.1:n.447+18A>G
ENST00000418967.6:c.447+18A>G	ENSP00000408860.2:n.447+18A>G
ENST00000435122.3:c.357+18A>G	ENSP00000415043.2:n.357+18A>G
ENST00000462278.1:n.35+18A>G
ENST00000464325.5:n.368+18A>G
ENST00000466779.5:c.*139+18A>G	ENSP00000417321.1:n.*139+18A>G
ENST00000466879.5:n.498+18A>G
ENST00000469053.5:c.*139+18A>G	ENSP00000418104.1:n.*139+18A>G
ENST00000471671.4:c.447+18A>G	ENSP00000418561.1:n.447+18A>G
ENST00000478281.5:c.480+18A>G	ENSP00000419572.1:n.480+18A>G
ENST00000479074.5:n.505+18A>G
ENST00000479730.5:n.602+18A>G
ENST00000483041.5:n.616+18A>G
ENST00000486063.5:n.627+18A>G
ENST00000488465.1:n.455+18A>G
NM_000500.7:c.447+18A>G	NP_000491.4:n.447+18A>G
NM_001128590.3:c.357+18A>G	NP_001122062.3:n.357+18A>G
XM_011514314.1:c.42+18A>G	XP_011512616.1:n.42+18A>G
NM_000500.9:c.447+18A>G MANE Select	NP_000491.4:n.447+18A>G
NM_001368143.1:c.42+18A>G	NP_001355072.1:n.42+18A>G
NM_001368144.1:c.42+18A>G	NP_001355073.1:n.42+18A>G
NM_001128590.4:c.357+18A>G	NP_001122062.3:n.357+18A>G
NM_001368143.2:c.42+18A>G	NP_001355072.1:n.42+18A>G
NM_001368144.2:c.42+18A>G	NP_001355073.1:n.42+18A>G