Canonical Allele Identifier: CA363512098

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008733T>A (hg19) ; chr6:g.32040956T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040956T>A , CM000668.2:g.32040956T>A	GRCh38
NC_000006.11:g.32008733T>A , CM000668.1:g.32008733T>A	GRCh37
NC_000006.10:g.32116712T>A	NCBI36
NG_007941.2:g.7649T>A
NG_008337.2:g.73419A>T
NG_007941.3:g.7652T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1310T>A MANE Select	ENSP00000496625.1:p.Leu437Gln
ENST00000418967.6:c.1310T>A	ENSP00000408860.2:p.Leu437Gln
ENST00000435122.3:c.1220T>A	ENSP00000415043.2:p.Leu407Gln
ENST00000479074.5:n.1451T>A
ENST00000479730.5:n.1426T>A
ENST00000483041.5:n.1479T>A
ENST00000486063.5:n.1289T>A
NM_000500.7:c.1310T>A	NP_000491.4:p.Leu437Gln
NM_001128590.3:c.1220T>A	NP_001122062.3:p.Leu407Gln
XM_011514314.1:c.905T>A	XP_011512616.1:p.Leu302Gln
NM_000500.9:c.1310T>A MANE Select	NP_000491.4:p.Leu437Gln
NM_001368143.1:c.905T>A	NP_001355072.1:p.Leu302Gln
NM_001368144.1:c.905T>A	NP_001355073.1:p.Leu302Gln
NM_001128590.4:c.1220T>A	NP_001122062.3:p.Leu407Gln
NM_001368143.2:c.905T>A	NP_001355072.1:p.Leu302Gln
NM_001368144.2:c.905T>A	NP_001355073.1:p.Leu302Gln