Canonical Allele Identifier: CA2678089067

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32040264-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040267del , CM000668.2:g.32040267del	GRCh38
NC_000006.11:g.32008044del , CM000668.1:g.32008044del	GRCh37
NC_000006.10:g.32116023del	NCBI36
NG_007941.2:g.6960del
NG_008337.2:g.74110del
NG_007941.3:g.6963del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.939+62del MANE Select	ENSP00000496625.1:n.939+62del
ENST00000418967.6:c.939+62del	ENSP00000408860.2:n.939+62del
ENST00000435122.3:c.849+62del	ENSP00000415043.2:n.849+62del
ENST00000479074.5:n.997+62del
ENST00000479730.5:n.1055+62del
ENST00000483041.5:n.1108+62del
ENST00000486063.5:n.919-139del
NM_000500.7:c.939+62del	NP_000491.4:n.939+62del
NM_001128590.3:c.849+62del	NP_001122062.3:n.849+62del
XM_011514314.1:c.534+62del	XP_011512616.1:n.534+62del
NM_000500.9:c.939+62del MANE Select	NP_000491.4:n.939+62del
NM_001368143.1:c.534+62del	NP_001355072.1:n.534+62del
NM_001368144.1:c.534+62del	NP_001355073.1:n.534+62del
NM_001128590.4:c.849+62del	NP_001122062.3:n.849+62del
NM_001368143.2:c.534+62del	NP_001355072.1:n.534+62del
NM_001368144.2:c.534+62del	NP_001355073.1:n.534+62del