Canonical Allele Identifier: CA363504145

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007399T>A (hg19) ; chr6:g.32039622T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039622T>A , CM000668.2:g.32039622T>A	GRCh38
NC_000006.11:g.32007399T>A , CM000668.1:g.32007399T>A	GRCh37
NC_000006.10:g.32115378T>A	NCBI36
NG_007941.2:g.6315T>A
NG_008337.2:g.74753A>T
NG_007941.3:g.6318T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.626T>A MANE Select	ENSP00000496625.1:p.Ile209Asn
ENST00000418967.6:c.626T>A	ENSP00000408860.2:p.Ile209Asn
ENST00000435122.3:c.536T>A	ENSP00000415043.2:p.Ile179Asn
ENST00000462278.1:n.214T>A
ENST00000464325.5:n.547T>A
ENST00000466779.5:c.*318T>A	ENSP00000417321.1:n.*318T>A
ENST00000466879.5:n.677T>A
ENST00000469053.5:c.*318T>A	ENSP00000418104.1:n.*318T>A
ENST00000479074.5:n.684T>A
ENST00000479730.5:n.742T>A
ENST00000483041.5:n.795T>A
ENST00000486063.5:n.806T>A
NM_000500.7:c.626T>A	NP_000491.4:p.Ile209Asn
NM_001128590.3:c.536T>A	NP_001122062.3:p.Ile179Asn
XM_011514314.1:c.221T>A	XP_011512616.1:p.Ile74Asn
NM_000500.9:c.626T>A MANE Select	NP_000491.4:p.Ile209Asn
NM_001368143.1:c.221T>A	NP_001355072.1:p.Ile74Asn
NM_001368144.1:c.221T>A	NP_001355073.1:p.Ile74Asn
NM_001128590.4:c.536T>A	NP_001122062.3:p.Ile179Asn
NM_001368143.2:c.221T>A	NP_001355072.1:p.Ile74Asn
NM_001368144.2:c.221T>A	NP_001355073.1:p.Ile74Asn