Canonical Allele Identifier: CA2678088521
Gene: CYP21A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038913_32038914insCA , CM000668.2:g.32038913_32038914insCA GRCh38
NC_000006.11:g.32006690_32006691insCA , CM000668.1:g.32006690_32006691insCA GRCh37
NC_000006.10:g.32114669_32114670insCA NCBI36
NG_007941.2:g.5606_5607insCA
NG_007941.3:g.5609_5610insCA

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.292+102_292+103insCA MANE Select ENSP00000496625.1:n.292+102_292+103insCA
ENST00000418967.6:c.292+102_292+103insCA ENSP00000408860.2:n.292+102_292+103insCA
ENST00000435122.3:c.203-181_203-180insCA ENSP00000415043.2:n.203-181_203-180insCA
ENST00000464325.5:n.229+102_229+103insCA
ENST00000466779.5:c.292+102_292+103insCA ENSP00000417321.1:n.292+102_292+103insCA
ENST00000466879.5:n.163_164insCA
ENST00000469053.5:c.203-162_203-161insCA ENSP00000418104.1:n.203-162_203-161insCA
ENST00000471671.4:c.292+102_292+103insCA ENSP00000418561.1:n.292+102_292+103insCA
ENST00000478281.5:c.292+102_292+103insCA ENSP00000419572.1:n.292+102_292+103insCA
ENST00000479074.5:n.350+102_350+103insCA
ENST00000479730.5:n.447+102_447+103insCA
ENST00000480027.1:n.447_448insCA
ENST00000483041.5:n.442+102_442+103insCA
ENST00000486063.5:n.472+102_472+103insCA
ENST00000488465.1:n.300+102_300+103insCA
NM_000500.7:c.292+102_292+103insCA NP_000491.4:n.292+102_292+103insCA
NM_001128590.3:c.203-181_203-180insCA NP_001122062.3:n.203-181_203-180insCA
XM_011514314.1:c.-133+102_-133+103insCA XP_011512616.1:n.-133+102_-133+103insCA
NM_000500.9:c.292+102_292+103insCA MANE Select NP_000491.4:n.292+102_292+103insCA
NM_001368143.1:c.-133+102_-133+103insCA NP_001355072.1:n.-133+102_-133+103insCA
NM_001368144.1:c.-132-162_-132-161insCA NP_001355073.1:n.-132-162_-132-161insCA
NM_001128590.4:c.203-181_203-180insCA NP_001122062.3:n.203-181_203-180insCA
NM_001368143.2:c.-133+102_-133+103insCA NP_001355072.1:n.-133+102_-133+103insCA
NM_001368144.2:c.-132-162_-132-161insCA NP_001355073.1:n.-132-162_-132-161insCA