Canonical Allele Identifier: CA363512008
Gene: CYP21A2 HGNC NCBI

Linked Data

dbSNP Id: rs1245238711
gnomAD v2: 6-32008717-G-A
gnomAD v3: 6-32040940-G-A
gnomAD v4: 6-32040940-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040940G>A , CM000668.2:g.32040940G>A GRCh38
NC_000006.11:g.32008717G>A , CM000668.1:g.32008717G>A GRCh37
NC_000006.10:g.32116696G>A NCBI36
NG_007941.2:g.7633G>A
NG_008337.2:g.73435C>T
NG_007941.3:g.7636G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.1294G>A MANE Select ENSP00000496625.1:p.Glu432Lys
ENST00000418967.6:c.1294G>A ENSP00000408860.2:p.Glu432Lys
ENST00000435122.3:c.1204G>A ENSP00000415043.2:p.Glu402Lys
ENST00000479074.5:n.1435G>A
ENST00000479730.5:n.1410G>A
ENST00000483041.5:n.1463G>A
ENST00000486063.5:n.1273G>A
NM_000500.7:c.1294G>A NP_000491.4:p.Glu432Lys
NM_001128590.3:c.1204G>A NP_001122062.3:p.Glu402Lys
XM_011514314.1:c.889G>A XP_011512616.1:p.Glu297Lys
NM_000500.9:c.1294G>A MANE Select NP_000491.4:p.Glu432Lys
NM_001368143.1:c.889G>A NP_001355072.1:p.Glu297Lys
NM_001368144.1:c.889G>A NP_001355073.1:p.Glu297Lys
NM_001128590.4:c.1204G>A NP_001122062.3:p.Glu402Lys
NM_001368143.2:c.889G>A NP_001355072.1:p.Glu297Lys
NM_001368144.2:c.889G>A NP_001355073.1:p.Glu297Lys