Canonical Allele Identifier: CA1619399394
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040774A= , CM000668.2:g.32040774A= GRCh38
NC_000006.11:g.32008551A= , CM000668.1:g.32008551A= GRCh37
NC_000006.10:g.32116530A= NCBI36
NG_007941.2:g.7467A=
NG_008337.2:g.73601T=
NG_007941.3:g.7470A=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.1222+3A= MANE Select ENSP00000496625.1:n.1222+3A=
ENST00000418967.6:c.1222+3A= ENSP00000408860.2:n.1222+3A=
ENST00000435122.3:c.1132+3A= ENSP00000415043.2:n.1132+3A=
ENST00000479074.5:n.1363+3A=
ENST00000479730.5:n.1338+3A=
ENST00000483041.5:n.1391+3A=
ENST00000486063.5:n.1201+3A=
NM_000500.7:c.1222+3A= NP_000491.4:n.1222+3A=
NM_001128590.3:c.1132+3A= NP_001122062.3:n.1132+3A=
XM_011514314.1:c.817+3A= XP_011512616.1:n.817+3A=
NM_000500.9:c.1222+3A= MANE Select NP_000491.4:n.1222+3A=
NM_001368143.1:c.817+3A= NP_001355072.1:n.817+3A=
NM_001368144.1:c.817+3A= NP_001355073.1:n.817+3A=
NM_001128590.4:c.1132+3A= NP_001122062.3:n.1132+3A=
NM_001368143.2:c.817+3A= NP_001355072.1:n.817+3A=
NM_001368144.2:c.817+3A= NP_001355073.1:n.817+3A=