Canonical Allele Identifier: CA2678090609
Gene: CYP21A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32041012_32041029del , CM000668.2:g.32041012_32041029del GRCh38
NC_000006.11:g.32008789_32008806del , CM000668.1:g.32008789_32008806del GRCh37
NC_000006.10:g.32116768_32116785del NCBI36
NG_007941.2:g.7705_7722del
NG_008337.2:g.73355_73372del
NG_007941.3:g.7708_7725del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.1366_1383del MANE Select ENSP00000496625.1:p.Gly456_Ser461del
ENST00000418967.6:c.1366_1383del ENSP00000408860.2:p.Gly456_Ser461del
ENST00000435122.3:c.1276_1293del ENSP00000415043.2:p.Gly426_Ser431del
ENST00000479074.5:n.1507_1524del
ENST00000479730.5:n.1482_1499del
ENST00000483041.5:n.1535_1552del
ENST00000486063.5:n.1345_1362del
NM_000500.7:c.1366_1383del NP_000491.4:p.Gly456_Ser461del
NM_001128590.3:c.1276_1293del NP_001122062.3:p.Gly426_Ser431del
XM_011514314.1:c.961_978del XP_011512616.1:p.Gly321_Ser326del
NM_000500.9:c.1366_1383del MANE Select NP_000491.4:p.Gly456_Ser461del
NM_001368143.1:c.961_978del NP_001355072.1:p.Gly321_Ser326del
NM_001368144.1:c.961_978del NP_001355073.1:p.Gly321_Ser326del
NM_001128590.4:c.1276_1293del NP_001122062.3:p.Gly426_Ser431del
NM_001368143.2:c.961_978del NP_001355072.1:p.Gly321_Ser326del
NM_001368144.2:c.961_978del NP_001355073.1:p.Gly321_Ser326del