Canonical Allele Identifier: CA2578574244

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32041144A>T , CM000668.2:g.32041144A>T	GRCh38
NC_000006.11:g.32008921A>T , CM000668.1:g.32008921A>T	GRCh37
NC_000006.10:g.32116900A>T	NCBI36
NG_007941.2:g.7837A>T
NG_008337.2:g.73231T>A
NG_007941.3:g.7840A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.*10A>T MANE Select	ENSP00000496625.1:n.*10A>T
ENST00000418967.6:c.*10A>T	ENSP00000408860.2:n.*10A>T
ENST00000435122.3:c.*10A>T	ENSP00000415043.2:n.*10A>T
ENST00000479074.5:n.1639A>T
ENST00000479730.5:n.1614A>T
ENST00000483041.5:n.1667A>T
ENST00000486063.5:n.1477A>T
NM_000500.7:c.*10A>T	NP_000491.4:n.*10A>T
NM_001128590.3:c.*10A>T	NP_001122062.3:n.*10A>T
XM_011514314.1:c.*10A>T	XP_011512616.1:n.*10A>T
NM_000500.9:c.*10A>T MANE Select	NP_000491.4:n.*10A>T
NM_001368143.1:c.*10A>T	NP_001355072.1:n.*10A>T
NM_001368144.1:c.*10A>T	NP_001355073.1:n.*10A>T
NM_001128590.4:c.*10A>T	NP_001122062.3:n.*10A>T
NM_001368143.2:c.*10A>T	NP_001355072.1:n.*10A>T
NM_001368144.2:c.*10A>T	NP_001355073.1:n.*10A>T