Canonical Allele Identifier: CA2678088601
Gene: CYP21A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038979_32038980insATA , CM000668.2:g.32038979_32038980insATA GRCh38
NC_000006.11:g.32006756_32006757insATA , CM000668.1:g.32006756_32006757insATA GRCh37
NC_000006.10:g.32114735_32114736insATA NCBI36
NG_007941.2:g.5672_5673insATA
NG_007941.3:g.5675_5676insATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.293-115_293-114insATA MANE Select ENSP00000496625.1:n.293-115_293-114insATA
ENST00000418967.6:c.293-115_293-114insATA ENSP00000408860.2:n.293-115_293-114insATA
ENST00000435122.3:c.203-115_203-114insATA ENSP00000415043.2:n.203-115_203-114insATA
ENST00000464325.5:n.230-131_230-130insATA
ENST00000466779.5:c.293-96_293-95insATA ENSP00000417321.1:n.293-96_293-95insATA
ENST00000466879.5:n.229_230insATA
ENST00000469053.5:c.203-96_203-95insATA ENSP00000418104.1:n.203-96_203-95insATA
ENST00000471671.4:c.293-115_293-114insATA ENSP00000418561.1:n.293-115_293-114insATA
ENST00000478281.5:c.293-82_293-81insATA ENSP00000419572.1:n.293-82_293-81insATA
ENST00000479074.5:n.351-115_351-114insATA
ENST00000479730.5:n.448-115_448-114insATA
ENST00000480027.1:n.513_514insATA
ENST00000483041.5:n.443-96_443-95insATA
ENST00000486063.5:n.473-115_473-114insATA
ENST00000488465.1:n.301-115_301-114insATA
NM_000500.7:c.293-115_293-114insATA NP_000491.4:n.293-115_293-114insATA
NM_001128590.3:c.203-115_203-114insATA NP_001122062.3:n.203-115_203-114insATA
XM_011514314.1:c.-132-96_-132-95insATA XP_011512616.1:n.-132-96_-132-95insATA
NM_000500.9:c.293-115_293-114insATA MANE Select NP_000491.4:n.293-115_293-114insATA
NM_001368143.1:c.-132-96_-132-95insATA NP_001355072.1:n.-132-96_-132-95insATA
NM_001368144.1:c.-132-96_-132-95insATA NP_001355073.1:n.-132-96_-132-95insATA
NM_001128590.4:c.203-115_203-114insATA NP_001122062.3:n.203-115_203-114insATA
NM_001368143.2:c.-132-96_-132-95insATA NP_001355072.1:n.-132-96_-132-95insATA
NM_001368144.2:c.-132-96_-132-95insATA NP_001355073.1:n.-132-96_-132-95insATA