Canonical Allele Identifier: CA1619396917
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32039357G= , CM000668.2:g.32039357G= GRCh38
NC_000006.11:g.32007134G= , CM000668.1:g.32007134G= GRCh37
NC_000006.10:g.32115113G= NCBI36
NG_007941.2:g.6050G=
NG_008337.2:g.75018C=
NG_007941.3:g.6053G=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.449G= MANE Select ENSP00000496625.1:p.Arg150=
ENST00000418967.6:c.449G= ENSP00000408860.2:p.Arg150=
ENST00000435122.3:c.359G= ENSP00000415043.2:p.Arg120=
ENST00000462278.1:n.37G=
ENST00000464325.5:n.370G=
ENST00000466779.5:c.*141G= ENSP00000417321.1:n.*141G=
ENST00000466879.5:n.500G=
ENST00000469053.5:c.*141G= ENSP00000418104.1:n.*141G=
ENST00000471671.4:c.449G= ENSP00000418561.1:p.Arg150=
ENST00000478281.5:c.482G= ENSP00000419572.1:p.Arg161=
ENST00000479074.5:n.507G=
ENST00000479730.5:n.604G=
ENST00000483041.5:n.618G=
ENST00000486063.5:n.629G=
ENST00000488465.1:n.457G=
NM_000500.7:c.449G= NP_000491.4:p.Arg150=
NM_001128590.3:c.359G= NP_001122062.3:p.Arg120=
XM_011514314.1:c.44G= XP_011512616.1:p.Arg15=
NM_000500.9:c.449G= MANE Select NP_000491.4:p.Arg150=
NM_001368143.1:c.44G= NP_001355072.1:p.Arg15=
NM_001368144.1:c.44G= NP_001355073.1:p.Arg15=
NM_001128590.4:c.359G= NP_001122062.3:p.Arg120=
NM_001368143.2:c.44G= NP_001355072.1:p.Arg15=
NM_001368144.2:c.44G= NP_001355073.1:p.Arg15=