Canonical Allele Identifier: CA1619399297

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040588A= , CM000668.2:g.32040588A=	GRCh38
NC_000006.11:g.32008365A= , CM000668.1:g.32008365A=	GRCh37
NC_000006.10:g.32116344A=	NCBI36
NG_007941.2:g.7281A=
NG_008337.2:g.73787T=
NG_007941.3:g.7284A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1118+4A= MANE Select	ENSP00000496625.1:n.1118+4A=
ENST00000418967.6:c.1118+4A=	ENSP00000408860.2:n.1118+4A=
ENST00000435122.3:c.1028+4A=	ENSP00000415043.2:n.1028+4A=
ENST00000479074.5:n.1180A=
ENST00000479730.5:n.1234+4A=
ENST00000483041.5:n.1287+4A=
ENST00000486063.5:n.1097+4A=
NM_000500.7:c.1118+4A=	NP_000491.4:n.1118+4A=
NM_001128590.3:c.1028+4A=	NP_001122062.3:n.1028+4A=
XM_011514314.1:c.713+4A=	XP_011512616.1:n.713+4A=
NM_000500.9:c.1118+4A= MANE Select	NP_000491.4:n.1118+4A=
NM_001368143.1:c.713+4A=	NP_001355072.1:n.713+4A=
NM_001368144.1:c.713+4A=	NP_001355073.1:n.713+4A=
NM_001128590.4:c.1028+4A=	NP_001122062.3:n.1028+4A=
NM_001368143.2:c.713+4A=	NP_001355072.1:n.713+4A=
NM_001368144.2:c.713+4A=	NP_001355073.1:n.713+4A=