Canonical Allele Identifier: CA363503827
Gene: CYP21A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32039595A>G , CM000668.2:g.32039595A>G GRCh38
NC_000006.11:g.32007372A>G , CM000668.1:g.32007372A>G GRCh37
NC_000006.10:g.32115351A>G NCBI36
NG_007941.2:g.6288A>G
NG_008337.2:g.74780T>C
NG_007941.3:g.6291A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.599A>G MANE Select ENSP00000496625.1:p.Lys200Arg
ENST00000418967.6:c.599A>G ENSP00000408860.2:p.Lys200Arg
ENST00000435122.3:c.509A>G ENSP00000415043.2:p.Lys170Arg
ENST00000462278.1:n.187A>G
ENST00000464325.5:n.520A>G
ENST00000466779.5:c.*291A>G ENSP00000417321.1:n.*291A>G
ENST00000466879.5:n.650A>G
ENST00000469053.5:c.*291A>G ENSP00000418104.1:n.*291A>G
ENST00000471671.4:c.560A>G ENSP00000418561.1:p.Lys187Arg
ENST00000479074.5:n.657A>G
ENST00000479730.5:n.715A>G
ENST00000483041.5:n.768A>G
ENST00000486063.5:n.779A>G
NM_000500.7:c.599A>G NP_000491.4:p.Lys200Arg
NM_001128590.3:c.509A>G NP_001122062.3:p.Lys170Arg
XM_011514314.1:c.194A>G XP_011512616.1:p.Lys65Arg
NM_000500.9:c.599A>G MANE Select NP_000491.4:p.Lys200Arg
NM_001368143.1:c.194A>G NP_001355072.1:p.Lys65Arg
NM_001368144.1:c.194A>G NP_001355073.1:p.Lys65Arg
NM_001128590.4:c.509A>G NP_001122062.3:p.Lys170Arg
NM_001368143.2:c.194A>G NP_001355072.1:p.Lys65Arg
NM_001368144.2:c.194A>G NP_001355073.1:p.Lys65Arg