Canonical Allele Identifier: CA2187638135

Gene: CYP11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339853C= , CM000677.2:g.74339853C=	GRCh38
NC_000015.9:g.74632194C= , CM000677.1:g.74632194C=	GRCh37
NC_000015.8:g.72419247C=	NCBI36
NG_007973.1:g.32889G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.991-100G= MANE Select	ENSP00000268053.6:n.991-100G=
ENST00000268053.10:c.991-100G=	ENSP00000268053.6:n.991-100G=
ENST00000358632.8:c.517-100G=	ENSP00000351455.4:n.517-100G=
ENST00000435365.5:c.991-100G=	ENSP00000391081.1:n.991-100G=
ENST00000566674.5:c.517-100G=	ENSP00000456941.1:n.517-100G=
NM_000781.2:c.991-100G=	NP_000772.2:n.991-100G=
NM_001099773.1:c.517-100G=	NP_001093243.1:n.517-100G=
NM_000781.3:c.991-100G= MANE Select	NP_000772.2:n.991-100G=
NM_001099773.2:c.517-100G=	NP_001093243.1:n.517-100G=