Canonical Allele Identifier: CA2678088390

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32038791-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038792del , CM000668.2:g.32038792del	GRCh38
NC_000006.11:g.32006569del , CM000668.1:g.32006569del	GRCh37
NC_000006.10:g.32114548del	NCBI36
NG_007941.2:g.5485del
NG_007941.3:g.5488del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.273del MANE Select	ENSP00000496625.1:p.Arg92AspfsTer?
ENST00000418967.6:c.273del	ENSP00000408860.2:p.Arg92AspfsTer?
ENST00000435122.3:c.202+168del	ENSP00000415043.2:n.202+168del
ENST00000464325.5:n.210del
ENST00000466779.5:c.273del	ENSP00000417321.1:p.Arg92AspfsTer?
ENST00000466879.5:n.42del
ENST00000469053.5:c.202+168del	ENSP00000418104.1:n.202+168del
ENST00000471671.4:c.273del	ENSP00000418561.1:p.Arg92AspfsTer?
ENST00000478281.5:c.273del	ENSP00000419572.1:p.Arg92AspfsTer?
ENST00000479074.5:n.331del
ENST00000479730.5:n.428del
ENST00000480027.1:n.326del
ENST00000483041.5:n.423del
ENST00000486063.5:n.453del
ENST00000488465.1:n.281del
NM_000500.7:c.273del	NP_000491.4:p.Arg92AspfsTer?
NM_001128590.3:c.202+168del	NP_001122062.3:n.202+168del
XM_011514314.1:c.-152del	XP_011512616.1:n.-152del
NM_000500.9:c.273del MANE Select	NP_000491.4:p.Arg92AspfsTer?
NM_001368143.1:c.-152del	NP_001355072.1:n.-152del
NM_001368144.1:c.-133+168del	NP_001355073.1:n.-133+168del
NM_001128590.4:c.202+168del	NP_001122062.3:n.202+168del
NM_001368143.2:c.-152del	NP_001355072.1:n.-152del
NM_001368144.2:c.-133+168del	NP_001355073.1:n.-133+168del