Canonical Allele Identifier: CA2678088272

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32038421-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038421C>A , CM000668.2:g.32038421C>A	GRCh38
NC_000006.11:g.32006198C>A , CM000668.1:g.32006198C>A	GRCh37
NC_000006.10:g.32114177C>A	NCBI36
NG_007941.2:g.5117C>A
NG_007941.3:g.5117C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.-2C>A MANE Select	ENSP00000496625.1:n.-2C>A
ENST00000418967.6:c.-2C>A	ENSP00000408860.2:n.-2C>A
ENST00000435122.3:c.-2C>A	ENSP00000415043.2:n.-2C>A
ENST00000466779.5:c.-2C>A	ENSP00000417321.1:n.-2C>A
ENST00000469053.5:c.-2C>A	ENSP00000418104.1:n.-2C>A
ENST00000471671.4:c.-2C>A	ENSP00000418561.1:n.-2C>A
ENST00000478281.5:c.-2C>A	ENSP00000419572.1:n.-2C>A
ENST00000479074.5:n.57C>A
ENST00000479730.5:n.57C>A
ENST00000480027.1:n.52C>A
ENST00000483041.5:n.52C>A
ENST00000486063.5:n.82C>A
ENST00000488465.1:n.7C>A
NM_000500.7:c.-2C>A	NP_000491.4:n.-2C>A
NM_001128590.3:c.-2C>A	NP_001122062.3:n.-2C>A
XM_011514314.1:c.-426C>A	XP_011512616.1:n.-426C>A
NM_000500.9:c.-2C>A MANE Select	NP_000491.4:n.-2C>A
NM_001368143.1:c.-426C>A	NP_001355072.1:n.-426C>A
NM_001368144.1:c.-336C>A	NP_001355073.1:n.-336C>A
NM_001128590.4:c.-2C>A	NP_001122062.3:n.-2C>A
NM_001368143.2:c.-426C>A	NP_001355072.1:n.-426C>A
NM_001368144.2:c.-336C>A	NP_001355073.1:n.-336C>A