Canonical Allele Identifier: CA363502577

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007143C>G (hg19) ; chr6:g.32039366C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039366C>G , CM000668.2:g.32039366C>G	GRCh38
NC_000006.11:g.32007143C>G , CM000668.1:g.32007143C>G	GRCh37
NC_000006.10:g.32115122C>G	NCBI36
NG_007941.2:g.6059C>G
NG_008337.2:g.75009G>C
NG_007941.3:g.6062C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.458C>G MANE Select	ENSP00000496625.1:p.Ala153Gly
ENST00000418967.6:c.458C>G	ENSP00000408860.2:p.Ala153Gly
ENST00000435122.3:c.368C>G	ENSP00000415043.2:p.Ala123Gly
ENST00000462278.1:n.46C>G
ENST00000464325.5:n.379C>G
ENST00000466779.5:c.*150C>G	ENSP00000417321.1:n.*150C>G
ENST00000466879.5:n.509C>G
ENST00000469053.5:c.*150C>G	ENSP00000418104.1:n.*150C>G
ENST00000471671.4:c.458C>G	ENSP00000418561.1:p.Ala153Gly
ENST00000478281.5:c.491C>G	ENSP00000419572.1:p.Ala164Gly
ENST00000479074.5:n.516C>G
ENST00000479730.5:n.613C>G
ENST00000483041.5:n.627C>G
ENST00000486063.5:n.638C>G
ENST00000488465.1:n.466C>G
NM_000500.7:c.458C>G	NP_000491.4:p.Ala153Gly
NM_001128590.3:c.368C>G	NP_001122062.3:p.Ala123Gly
XM_011514314.1:c.53C>G	XP_011512616.1:p.Ala18Gly
NM_000500.9:c.458C>G MANE Select	NP_000491.4:p.Ala153Gly
NM_001368143.1:c.53C>G	NP_001355072.1:p.Ala18Gly
NM_001368144.1:c.53C>G	NP_001355073.1:p.Ala18Gly
NM_001128590.4:c.368C>G	NP_001122062.3:p.Ala123Gly
NM_001368143.2:c.53C>G	NP_001355072.1:p.Ala18Gly
NM_001368144.2:c.53C>G	NP_001355073.1:p.Ala18Gly