Canonical Allele Identifier: CA1619399251

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040500T= , CM000668.2:g.32040500T=	GRCh38
NC_000006.11:g.32008277T= , CM000668.1:g.32008277T=	GRCh37
NC_000006.10:g.32116256T=	NCBI36
NG_007941.2:g.7193T=
NG_008337.2:g.73875A=
NG_007941.3:g.7196T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1034T= MANE Select	ENSP00000496625.1:p.Leu345=
ENST00000418967.6:c.1034T=	ENSP00000408860.2:p.Leu345=
ENST00000435122.3:c.944T=	ENSP00000415043.2:p.Leu315=
ENST00000479074.5:n.1092T=
ENST00000479730.5:n.1150T=
ENST00000483041.5:n.1203T=
ENST00000486063.5:n.1013T=
NM_000500.7:c.1034T=	NP_000491.4:p.Leu345=
NM_001128590.3:c.944T=	NP_001122062.3:p.Leu315=
XM_011514314.1:c.629T=	XP_011512616.1:p.Leu210=
NM_000500.9:c.1034T= MANE Select	NP_000491.4:p.Leu345=
NM_001368143.1:c.629T=	NP_001355072.1:p.Leu210=
NM_001368144.1:c.629T=	NP_001355073.1:p.Leu210=
NM_001128590.4:c.944T=	NP_001122062.3:p.Leu315=
NM_001368143.2:c.629T=	NP_001355072.1:p.Leu210=
NM_001368144.2:c.629T=	NP_001355073.1:p.Leu210=