Canonical Allele Identifier: CA2678088333

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32038657-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038658dup , CM000668.2:g.32038658dup	GRCh38
NC_000006.11:g.32006435dup , CM000668.1:g.32006435dup	GRCh37
NC_000006.10:g.32114414dup	NCBI36
NG_007941.2:g.5351dup
NG_007941.3:g.5354dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.202+34dup MANE Select	ENSP00000496625.1:n.202+34dup
ENST00000418967.6:c.202+34dup	ENSP00000408860.2:n.202+34dup
ENST00000435122.3:c.202+34dup	ENSP00000415043.2:n.202+34dup
ENST00000464325.5:n.76dup
ENST00000466779.5:c.202+34dup	ENSP00000417321.1:n.202+34dup
ENST00000469053.5:c.202+34dup	ENSP00000418104.1:n.202+34dup
ENST00000471671.4:c.202+34dup	ENSP00000418561.1:n.202+34dup
ENST00000478281.5:c.202+34dup	ENSP00000419572.1:n.202+34dup
ENST00000479074.5:n.260+34dup
ENST00000479730.5:n.294dup
ENST00000480027.1:n.255+34dup
ENST00000483041.5:n.289dup
ENST00000486063.5:n.319dup
ENST00000488465.1:n.210+34dup
NM_000500.7:c.202+34dup	NP_000491.4:n.202+34dup
NM_001128590.3:c.202+34dup	NP_001122062.3:n.202+34dup
XM_011514314.1:c.-223+34dup	XP_011512616.1:n.-223+34dup
NM_000500.9:c.202+34dup MANE Select	NP_000491.4:n.202+34dup
NM_001368143.1:c.-223+34dup	NP_001355072.1:n.-223+34dup
NM_001368144.1:c.-133+34dup	NP_001355073.1:n.-133+34dup
NM_001128590.4:c.202+34dup	NP_001122062.3:n.202+34dup
NM_001368143.2:c.-223+34dup	NP_001355072.1:n.-223+34dup
NM_001368144.2:c.-133+34dup	NP_001355073.1:n.-133+34dup