Canonical Allele Identifier: CA2678088534

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32038923-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038923C>A , CM000668.2:g.32038923C>A	GRCh38
NC_000006.11:g.32006700C>A , CM000668.1:g.32006700C>A	GRCh37
NC_000006.10:g.32114679C>A	NCBI36
NG_007941.2:g.5616C>A
NG_007941.3:g.5619C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.292+112C>A MANE Select	ENSP00000496625.1:n.292+112C>A
ENST00000418967.6:c.292+112C>A	ENSP00000408860.2:n.292+112C>A
ENST00000435122.3:c.203-171C>A	ENSP00000415043.2:n.203-171C>A
ENST00000464325.5:n.229+112C>A
ENST00000466779.5:c.292+112C>A	ENSP00000417321.1:n.292+112C>A
ENST00000466879.5:n.173C>A
ENST00000469053.5:c.203-152C>A	ENSP00000418104.1:n.203-152C>A
ENST00000471671.4:c.292+112C>A	ENSP00000418561.1:n.292+112C>A
ENST00000478281.5:c.292+112C>A	ENSP00000419572.1:n.292+112C>A
ENST00000479074.5:n.350+112C>A
ENST00000479730.5:n.447+112C>A
ENST00000480027.1:n.457C>A
ENST00000483041.5:n.442+112C>A
ENST00000486063.5:n.472+112C>A
ENST00000488465.1:n.300+112C>A
NM_000500.7:c.292+112C>A	NP_000491.4:n.292+112C>A
NM_001128590.3:c.203-171C>A	NP_001122062.3:n.203-171C>A
XM_011514314.1:c.-133+112C>A	XP_011512616.1:n.-133+112C>A
NM_000500.9:c.292+112C>A MANE Select	NP_000491.4:n.292+112C>A
NM_001368143.1:c.-133+112C>A	NP_001355072.1:n.-133+112C>A
NM_001368144.1:c.-132-152C>A	NP_001355073.1:n.-132-152C>A
NM_001128590.4:c.203-171C>A	NP_001122062.3:n.203-171C>A
NM_001368143.2:c.-133+112C>A	NP_001355072.1:n.-133+112C>A
NM_001368144.2:c.-132-152C>A	NP_001355073.1:n.-132-152C>A