Canonical Allele Identifier: CA1619397307

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040084G= , CM000668.2:g.32040084G=	GRCh38
NC_000006.11:g.32007861G= , CM000668.1:g.32007861G=	GRCh37
NC_000006.10:g.32115840G=	NCBI36
NG_007941.2:g.6777G=
NG_008337.2:g.74291C=
NG_007941.3:g.6780G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.818G= MANE Select	ENSP00000496625.1:p.Gly273=
ENST00000418967.6:c.818G=	ENSP00000408860.2:p.Gly273=
ENST00000435122.3:c.728G=	ENSP00000415043.2:p.Gly243=
ENST00000479074.5:n.876G=
ENST00000479730.5:n.934G=
ENST00000483041.5:n.987G=
ENST00000486063.5:n.918+249G=
NM_000500.7:c.818G=	NP_000491.4:p.Gly273=
NM_001128590.3:c.728G=	NP_001122062.3:p.Gly243=
XM_011514314.1:c.413G=	XP_011512616.1:p.Gly138=
NM_000500.9:c.818G= MANE Select	NP_000491.4:p.Gly273=
NM_001368143.1:c.413G=	NP_001355072.1:p.Gly138=
NM_001368144.1:c.413G=	NP_001355073.1:p.Gly138=
NM_001128590.4:c.728G=	NP_001122062.3:p.Gly243=
NM_001368143.2:c.413G=	NP_001355072.1:p.Gly138=
NM_001368144.2:c.413G=	NP_001355073.1:p.Gly138=