Canonical Allele Identifier: CA1619399607

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32041041G= , CM000668.2:g.32041041G=	GRCh38
NC_000006.11:g.32008818G= , CM000668.1:g.32008818G=	GRCh37
NC_000006.10:g.32116797G=	NCBI36
NG_007941.2:g.7734G=
NG_008337.2:g.73334C=
NG_007941.3:g.7737G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1395G= MANE Select	ENSP00000496625.1:p.Leu465=
ENST00000418967.6:c.1395G=	ENSP00000408860.2:p.Leu465=
ENST00000435122.3:c.1305G=	ENSP00000415043.2:p.Leu435=
ENST00000479074.5:n.1536G=
ENST00000479730.5:n.1511G=
ENST00000483041.5:n.1564G=
ENST00000486063.5:n.1374G=
NM_000500.7:c.1395G=	NP_000491.4:p.Leu465=
NM_001128590.3:c.1305G=	NP_001122062.3:p.Leu435=
XM_011514314.1:c.990G=	XP_011512616.1:p.Leu330=
NM_000500.9:c.1395G= MANE Select	NP_000491.4:p.Leu465=
NM_001368143.1:c.990G=	NP_001355072.1:p.Leu330=
NM_001368144.1:c.990G=	NP_001355073.1:p.Leu330=
NM_001128590.4:c.1305G=	NP_001122062.3:p.Leu435=
NM_001368143.2:c.990G=	NP_001355072.1:p.Leu330=
NM_001368144.2:c.990G=	NP_001355073.1:p.Leu330=