Canonical Allele Identifier: CA1619397338

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040166C= , CM000668.2:g.32040166C=	GRCh38
NC_000006.11:g.32007943C= , CM000668.1:g.32007943C=	GRCh37
NC_000006.10:g.32115922C=	NCBI36
NG_007941.2:g.6859C=
NG_008337.2:g.74209G=
NG_007941.3:g.6862C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.900C= MANE Select	ENSP00000496625.1:p.Thr300=
ENST00000418967.6:c.900C=	ENSP00000408860.2:p.Thr300=
ENST00000435122.3:c.810C=	ENSP00000415043.2:p.Thr270=
ENST00000479074.5:n.958C=
ENST00000479730.5:n.1016C=
ENST00000483041.5:n.1069C=
ENST00000486063.5:n.919-240C=
NM_000500.7:c.900C=	NP_000491.4:p.Thr300=
NM_001128590.3:c.810C=	NP_001122062.3:p.Thr270=
XM_011514314.1:c.495C=	XP_011512616.1:p.Thr165=
NM_000500.9:c.900C= MANE Select	NP_000491.4:p.Thr300=
NM_001368143.1:c.495C=	NP_001355072.1:p.Thr165=
NM_001368144.1:c.495C=	NP_001355073.1:p.Thr165=
NM_001128590.4:c.810C=	NP_001122062.3:p.Thr270=
NM_001368143.2:c.495C=	NP_001355072.1:p.Thr165=
NM_001368144.2:c.495C=	NP_001355073.1:p.Thr165=