Canonical Allele Identifier: CA1619396918
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32039359A= , CM000668.2:g.32039359A= GRCh38
NC_000006.11:g.32007136A= , CM000668.1:g.32007136A= GRCh37
NC_000006.10:g.32115115A= NCBI36
NG_007941.2:g.6052A=
NG_008337.2:g.75016T=
NG_007941.3:g.6055A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.451A= MANE Select ENSP00000496625.1:p.Met151=
ENST00000418967.6:c.451A= ENSP00000408860.2:p.Met151=
ENST00000435122.3:c.361A= ENSP00000415043.2:p.Met121=
ENST00000462278.1:n.39A=
ENST00000464325.5:n.372A=
ENST00000466779.5:c.*143A= ENSP00000417321.1:n.*143A=
ENST00000466879.5:n.502A=
ENST00000469053.5:c.*143A= ENSP00000418104.1:n.*143A=
ENST00000471671.4:c.451A= ENSP00000418561.1:p.Met151=
ENST00000478281.5:c.484A= ENSP00000419572.1:p.Met162=
ENST00000479074.5:n.509A=
ENST00000479730.5:n.606A=
ENST00000483041.5:n.620A=
ENST00000486063.5:n.631A=
ENST00000488465.1:n.459A=
NM_000500.7:c.451A= NP_000491.4:p.Met151=
NM_001128590.3:c.361A= NP_001122062.3:p.Met121=
XM_011514314.1:c.46A= XP_011512616.1:p.Met16=
NM_000500.9:c.451A= MANE Select NP_000491.4:p.Met151=
NM_001368143.1:c.46A= NP_001355072.1:p.Met16=
NM_001368144.1:c.46A= NP_001355073.1:p.Met16=
NM_001128590.4:c.361A= NP_001122062.3:p.Met121=
NM_001368143.2:c.46A= NP_001355072.1:p.Met16=
NM_001368144.2:c.46A= NP_001355073.1:p.Met16=