Canonical Allele Identifier: CA363505178

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007578A>C (hg19) ; chr6:g.32039801A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039801A>C , CM000668.2:g.32039801A>C	GRCh38
NC_000006.11:g.32007578A>C , CM000668.1:g.32007578A>C	GRCh37
NC_000006.10:g.32115557A>C	NCBI36
NG_007941.2:g.6494A>C
NG_008337.2:g.74574T>G
NG_007941.3:g.6497A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.704A>C MANE Select	ENSP00000496625.1:p.Asp235Ala
ENST00000418967.6:c.704A>C	ENSP00000408860.2:p.Asp235Ala
ENST00000435122.3:c.614A>C	ENSP00000415043.2:p.Asp205Ala
ENST00000462278.1:n.393A>C
ENST00000466779.5:c.*396A>C	ENSP00000417321.1:n.*396A>C
ENST00000466879.5:n.755A>C
ENST00000479074.5:n.762A>C
ENST00000479730.5:n.820A>C
ENST00000483041.5:n.873A>C
ENST00000486063.5:n.884A>C
NM_000500.7:c.704A>C	NP_000491.4:p.Asp235Ala
NM_001128590.3:c.614A>C	NP_001122062.3:p.Asp205Ala
XM_011514314.1:c.299A>C	XP_011512616.1:p.Asp100Ala
NM_000500.9:c.704A>C MANE Select	NP_000491.4:p.Asp235Ala
NM_001368143.1:c.299A>C	NP_001355072.1:p.Asp100Ala
NM_001368144.1:c.299A>C	NP_001355073.1:p.Asp100Ala
NM_001128590.4:c.614A>C	NP_001122062.3:p.Asp205Ala
NM_001368143.2:c.299A>C	NP_001355072.1:p.Asp100Ala
NM_001368144.2:c.299A>C	NP_001355073.1:p.Asp100Ala