Canonical Allele Identifier: CA363510991

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008271T>A (hg19) ; chr6:g.32040494T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040494T>A , CM000668.2:g.32040494T>A	GRCh38
NC_000006.11:g.32008271T>A , CM000668.1:g.32008271T>A	GRCh37
NC_000006.10:g.32116250T>A	NCBI36
NG_007941.2:g.7187T>A
NG_008337.2:g.73881A>T
NG_007941.3:g.7190T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1028T>A MANE Select	ENSP00000496625.1:p.Leu343Gln
ENST00000418967.6:c.1028T>A	ENSP00000408860.2:p.Leu343Gln
ENST00000435122.3:c.938T>A	ENSP00000415043.2:p.Leu313Gln
ENST00000479074.5:n.1086T>A
ENST00000479730.5:n.1144T>A
ENST00000483041.5:n.1197T>A
ENST00000486063.5:n.1007T>A
NM_000500.7:c.1028T>A	NP_000491.4:p.Leu343Gln
NM_001128590.3:c.938T>A	NP_001122062.3:p.Leu313Gln
XM_011514314.1:c.623T>A	XP_011512616.1:p.Leu208Gln
NM_000500.9:c.1028T>A MANE Select	NP_000491.4:p.Leu343Gln
NM_001368143.1:c.623T>A	NP_001355072.1:p.Leu208Gln
NM_001368144.1:c.623T>A	NP_001355073.1:p.Leu208Gln
NM_001128590.4:c.938T>A	NP_001122062.3:p.Leu313Gln
NM_001368143.2:c.623T>A	NP_001355072.1:p.Leu208Gln
NM_001368144.2:c.623T>A	NP_001355073.1:p.Leu208Gln