Canonical Allele Identifier: CA363505743
Gene: CYP21A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040009G>A , CM000668.2:g.32040009G>A GRCh38
NC_000006.11:g.32007786G>A , CM000668.1:g.32007786G>A GRCh37
NC_000006.10:g.32115765G>A NCBI36
NG_007941.2:g.6702G>A
NG_008337.2:g.74366C>T
NG_007941.3:g.6705G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.743G>A MANE Select ENSP00000496625.1:p.Ser248Asn
ENST00000418967.6:c.743G>A ENSP00000408860.2:p.Ser248Asn
ENST00000435122.3:c.653G>A ENSP00000415043.2:p.Ser218Asn
ENST00000479074.5:n.801G>A
ENST00000479730.5:n.859G>A
ENST00000483041.5:n.912G>A
ENST00000486063.5:n.918+174G>A
NM_000500.7:c.743G>A NP_000491.4:p.Ser248Asn
NM_001128590.3:c.653G>A NP_001122062.3:p.Ser218Asn
XM_011514314.1:c.338G>A XP_011512616.1:p.Ser113Asn
NM_000500.9:c.743G>A MANE Select NP_000491.4:p.Ser248Asn
NM_001368143.1:c.338G>A NP_001355072.1:p.Ser113Asn
NM_001368144.1:c.338G>A NP_001355073.1:p.Ser113Asn
NM_001128590.4:c.653G>A NP_001122062.3:p.Ser218Asn
NM_001368143.2:c.338G>A NP_001355072.1:p.Ser113Asn
NM_001368144.2:c.338G>A NP_001355073.1:p.Ser113Asn