Canonical Allele Identifier: CA363511317

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008494C>G (hg19) ; chr6:g.32040717C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040717C>G , CM000668.2:g.32040717C>G	GRCh38
NC_000006.11:g.32008494C>G , CM000668.1:g.32008494C>G	GRCh37
NC_000006.10:g.32116473C>G	NCBI36
NG_007941.2:g.7410C>G
NG_008337.2:g.73658G>C
NG_007941.3:g.7413C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1168C>G MANE Select	ENSP00000496625.1:p.Gln390Glu
ENST00000418967.6:c.1168C>G	ENSP00000408860.2:p.Gln390Glu
ENST00000435122.3:c.1078C>G	ENSP00000415043.2:p.Gln360Glu
ENST00000479074.5:n.1309C>G
ENST00000479730.5:n.1284C>G
ENST00000483041.5:n.1337C>G
ENST00000486063.5:n.1147C>G
NM_000500.7:c.1168C>G	NP_000491.4:p.Gln390Glu
NM_001128590.3:c.1078C>G	NP_001122062.3:p.Gln360Glu
XM_011514314.1:c.763C>G	XP_011512616.1:p.Gln255Glu
NM_000500.9:c.1168C>G MANE Select	NP_000491.4:p.Gln390Glu
NM_001368143.1:c.763C>G	NP_001355072.1:p.Gln255Glu
NM_001368144.1:c.763C>G	NP_001355073.1:p.Gln255Glu
NM_001128590.4:c.1078C>G	NP_001122062.3:p.Gln360Glu
NM_001368143.2:c.763C>G	NP_001355072.1:p.Gln255Glu
NM_001368144.2:c.763C>G	NP_001355073.1:p.Gln255Glu