Canonical Allele Identifier: CA363511983

Gene: CYP21A2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040934C>G , CM000668.2:g.32040934C>G	GRCh38
NC_000006.11:g.32008711C>G , CM000668.1:g.32008711C>G	GRCh37
NC_000006.10:g.32116690C>G	NCBI36
NG_007941.2:g.7627C>G
NG_008337.2:g.73441G>C
NG_007941.3:g.7630C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1288C>G MANE Select	ENSP00000496625.1:p.Leu430Val
ENST00000418967.6:c.1288C>G	ENSP00000408860.2:p.Leu430Val
ENST00000435122.3:c.1198C>G	ENSP00000415043.2:p.Leu400Val
ENST00000479074.5:n.1429C>G
ENST00000479730.5:n.1404C>G
ENST00000483041.5:n.1457C>G
ENST00000486063.5:n.1267C>G
NM_000500.7:c.1288C>G	NP_000491.4:p.Leu430Val
NM_001128590.3:c.1198C>G	NP_001122062.3:p.Leu400Val
XM_011514314.1:c.883C>G	XP_011512616.1:p.Leu295Val
NM_000500.9:c.1288C>G MANE Select	NP_000491.4:p.Leu430Val
NM_001368143.1:c.883C>G	NP_001355072.1:p.Leu295Val
NM_001368144.1:c.883C>G	NP_001355073.1:p.Leu295Val
NM_001128590.4:c.1198C>G	NP_001122062.3:p.Leu400Val
NM_001368143.2:c.883C>G	NP_001355072.1:p.Leu295Val
NM_001368144.2:c.883C>G	NP_001355073.1:p.Leu295Val