Canonical Allele Identifier: CA363504824

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007553C>A (hg19) ; chr6:g.32039776C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039776C>A , CM000668.2:g.32039776C>A	GRCh38
NC_000006.11:g.32007553C>A , CM000668.1:g.32007553C>A	GRCh37
NC_000006.10:g.32115532C>A	NCBI36
NG_007941.2:g.6469C>A
NG_008337.2:g.74599G>T
NG_007941.3:g.6472C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.679C>A MANE Select	ENSP00000496625.1:p.Leu227Met
ENST00000418967.6:c.679C>A	ENSP00000408860.2:p.Leu227Met
ENST00000435122.3:c.589C>A	ENSP00000415043.2:p.Leu197Met
ENST00000462278.1:n.368C>A
ENST00000466779.5:c.*371C>A	ENSP00000417321.1:n.*371C>A
ENST00000466879.5:n.730C>A
ENST00000479074.5:n.737C>A
ENST00000479730.5:n.795C>A
ENST00000483041.5:n.848C>A
ENST00000486063.5:n.859C>A
NM_000500.7:c.679C>A	NP_000491.4:p.Leu227Met
NM_001128590.3:c.589C>A	NP_001122062.3:p.Leu197Met
XM_011514314.1:c.274C>A	XP_011512616.1:p.Leu92Met
NM_000500.9:c.679C>A MANE Select	NP_000491.4:p.Leu227Met
NM_001368143.1:c.274C>A	NP_001355072.1:p.Leu92Met
NM_001368144.1:c.274C>A	NP_001355073.1:p.Leu92Met
NM_001128590.4:c.589C>A	NP_001122062.3:p.Leu197Met
NM_001368143.2:c.274C>A	NP_001355072.1:p.Leu92Met
NM_001368144.2:c.274C>A	NP_001355073.1:p.Leu92Met