Canonical Allele Identifier: CA2187637886

Gene: CYP11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339608G= , CM000677.2:g.74339608G=	GRCh38
NC_000015.9:g.74631949G= , CM000677.1:g.74631949G=	GRCh37
NC_000015.8:g.72419002G=	NCBI36
NG_007973.1:g.33134C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000268053.11:c.1136C= MANE Select	ENSP00000268053.6:p.Ala379=
ENST00000268053.10:c.1136C=	ENSP00000268053.6:p.Ala379=
ENST00000358632.8:c.662C=	ENSP00000351455.4:p.Ala221=
ENST00000435365.5:c.1136C=	ENSP00000391081.1:p.Ala379=
ENST00000566674.5:c.662C=	ENSP00000456941.1:p.Ala221=
NM_000781.2:c.1136C=	NP_000772.2:p.Ala379=
NM_001099773.1:c.662C=	NP_001093243.1:p.Ala221=
NM_000781.3:c.1136C= MANE Select	NP_000772.2:p.Ala379=
NM_001099773.2:c.662C=	NP_001093243.1:p.Ala221=