Canonical Allele Identifier: CA1619396774
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32039101G= , CM000668.2:g.32039101G= GRCh38
NC_000006.11:g.32006878G= , CM000668.1:g.32006878G= GRCh37
NC_000006.10:g.32114857G= NCBI36
NG_007941.2:g.5794G=
NG_007941.3:g.5797G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.300G= MANE Select ENSP00000496625.1:p.Leu100=
ENST00000418967.6:c.300G= ENSP00000408860.2:p.Leu100=
ENST00000435122.3:c.210G= ENSP00000415043.2:p.Leu70=
ENST00000464325.5:n.230-9G=
ENST00000466779.5:c.319G= ENSP00000417321.1:p.Gly107=
ENST00000466879.5:n.351G=
ENST00000469053.5:c.229G= ENSP00000418104.1:p.Gly77=
ENST00000471671.4:c.300G= ENSP00000418561.1:p.Leu100=
ENST00000478281.5:c.333G= ENSP00000419572.1:p.Leu111=
ENST00000479074.5:n.358G=
ENST00000479730.5:n.455G=
ENST00000480027.1:n.635G=
ENST00000483041.5:n.469G=
ENST00000486063.5:n.480G=
ENST00000488465.1:n.308G=
NM_000500.7:c.300G= NP_000491.4:p.Leu100=
NM_001128590.3:c.210G= NP_001122062.3:p.Leu70=
XM_011514314.1:c.-106G= XP_011512616.1:n.-106G=
NM_000500.9:c.300G= MANE Select NP_000491.4:p.Leu100=
NM_001368143.1:c.-106G= NP_001355072.1:n.-106G=
NM_001368144.1:c.-106G= NP_001355073.1:n.-106G=
NM_001128590.4:c.210G= NP_001122062.3:p.Leu70=
NM_001368143.2:c.-106G= NP_001355072.1:n.-106G=
NM_001368144.2:c.-106G= NP_001355073.1:n.-106G=