Canonical Allele Identifier: CA1619397350

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040183T= , CM000668.2:g.32040183T=	GRCh38
NC_000006.11:g.32007960T= , CM000668.1:g.32007960T=	GRCh37
NC_000006.10:g.32115939T=	NCBI36
NG_007941.2:g.6876T=
NG_008337.2:g.74192A=
NG_007941.3:g.6879T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.917T= MANE Select	ENSP00000496625.1:p.Val306=
ENST00000418967.6:c.917T=	ENSP00000408860.2:p.Val306=
ENST00000435122.3:c.827T=	ENSP00000415043.2:p.Val276=
ENST00000479074.5:n.975T=
ENST00000479730.5:n.1033T=
ENST00000483041.5:n.1086T=
ENST00000486063.5:n.919-223T=
NM_000500.7:c.917T=	NP_000491.4:p.Val306=
NM_001128590.3:c.827T=	NP_001122062.3:p.Val276=
XM_011514314.1:c.512T=	XP_011512616.1:p.Val171=
NM_000500.9:c.917T= MANE Select	NP_000491.4:p.Val306=
NM_001368143.1:c.512T=	NP_001355072.1:p.Val171=
NM_001368144.1:c.512T=	NP_001355073.1:p.Val171=
NM_001128590.4:c.827T=	NP_001122062.3:p.Val276=
NM_001368143.2:c.512T=	NP_001355072.1:p.Val171=
NM_001368144.2:c.512T=	NP_001355073.1:p.Val171=