Canonical Allele Identifier: CA2678090829

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32041140-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32041140C>A , CM000668.2:g.32041140C>A	GRCh38
NC_000006.11:g.32008917C>A , CM000668.1:g.32008917C>A	GRCh37
NC_000006.10:g.32116896C>A	NCBI36
NG_007941.2:g.7833C>A
NG_008337.2:g.73235G>T
NG_007941.3:g.7836C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.*6C>A MANE Select	ENSP00000496625.1:n.*6C>A
ENST00000418967.6:c.*6C>A	ENSP00000408860.2:n.*6C>A
ENST00000435122.3:c.*6C>A	ENSP00000415043.2:n.*6C>A
ENST00000479074.5:n.1635C>A
ENST00000479730.5:n.1610C>A
ENST00000483041.5:n.1663C>A
ENST00000486063.5:n.1473C>A
NM_000500.7:c.*6C>A	NP_000491.4:n.*6C>A
NM_001128590.3:c.*6C>A	NP_001122062.3:n.*6C>A
XM_011514314.1:c.*6C>A	XP_011512616.1:n.*6C>A
NM_000500.9:c.*6C>A MANE Select	NP_000491.4:n.*6C>A
NM_001368143.1:c.*6C>A	NP_001355072.1:n.*6C>A
NM_001368144.1:c.*6C>A	NP_001355073.1:n.*6C>A
NM_001128590.4:c.*6C>A	NP_001122062.3:n.*6C>A
NM_001368143.2:c.*6C>A	NP_001355072.1:n.*6C>A
NM_001368144.2:c.*6C>A	NP_001355073.1:n.*6C>A