Canonical Allele Identifier: CA2187638020

Gene: CYP11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339725T= , CM000677.2:g.74339725T=	GRCh38
NC_000015.9:g.74632066T= , CM000677.1:g.74632066T=	GRCh37
NC_000015.8:g.72419119T=	NCBI36
NG_007973.1:g.33017A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.1019A= MANE Select	ENSP00000268053.6:p.Tyr340=
ENST00000268053.10:c.1019A=	ENSP00000268053.6:p.Tyr340=
ENST00000358632.8:c.545A=	ENSP00000351455.4:p.Tyr182=
ENST00000435365.5:c.1019A=	ENSP00000391081.1:p.Tyr340=
ENST00000566674.5:c.545A=	ENSP00000456941.1:p.Tyr182=
NM_000781.2:c.1019A=	NP_000772.2:p.Tyr340=
NM_001099773.1:c.545A=	NP_001093243.1:p.Tyr182=
NM_000781.3:c.1019A= MANE Select	NP_000772.2:p.Tyr340=
NM_001099773.2:c.545A=	NP_001093243.1:p.Tyr182=