Canonical Allele Identifier: CA2678089744

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32040635-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040637del , CM000668.2:g.32040637del	GRCh38
NC_000006.11:g.32008414del , CM000668.1:g.32008414del	GRCh37
NC_000006.10:g.32116393del	NCBI36
NG_007941.2:g.7330del
NG_008337.2:g.73739del
NG_007941.3:g.7333del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1119-31del MANE Select	ENSP00000496625.1:n.1119-31del
ENST00000418967.6:c.1119-31del	ENSP00000408860.2:n.1119-31del
ENST00000435122.3:c.1029-31del	ENSP00000415043.2:n.1029-31del
ENST00000479074.5:n.1229del
ENST00000479730.5:n.1235-31del
ENST00000483041.5:n.1288-31del
ENST00000486063.5:n.1098-31del
NM_000500.7:c.1119-31del	NP_000491.4:n.1119-31del
NM_001128590.3:c.1029-31del	NP_001122062.3:n.1029-31del
XM_011514314.1:c.714-31del	XP_011512616.1:n.714-31del
NM_000500.9:c.1119-31del MANE Select	NP_000491.4:n.1119-31del
NM_001368143.1:c.714-31del	NP_001355072.1:n.714-31del
NM_001368144.1:c.714-31del	NP_001355073.1:n.714-31del
NM_001128590.4:c.1029-31del	NP_001122062.3:n.1029-31del
NM_001368143.2:c.714-31del	NP_001355072.1:n.714-31del
NM_001368144.2:c.714-31del	NP_001355073.1:n.714-31del