Canonical Allele Identifier: CA2187643745

Gene: CYP11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74347927T= , CM000677.2:g.74347927T=	GRCh38
NC_000015.9:g.74640268T= , CM000677.1:g.74640268T=	GRCh37
NC_000015.8:g.72427321T=	NCBI36
NG_007973.1:g.24815A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.398A= MANE Select	ENSP00000268053.6:p.Tyr133=
ENST00000268053.10:c.398A=	ENSP00000268053.6:p.Tyr133=
ENST00000358632.8:c.-77A=	ENSP00000351455.4:n.-77A=
ENST00000416978.1:c.398A=	ENSP00000388018.1:p.Tyr133=
ENST00000435365.5:c.398A=	ENSP00000391081.1:p.Tyr133=
ENST00000450547.1:c.-77A=	ENSP00000402064.1:n.-77A=
ENST00000466978.1:n.792A=
ENST00000566674.5:c.-77A=	ENSP00000456941.1:n.-77A=
ENST00000569662.1:c.-49-2684A=	ENSP00000456598.1:n.-49-2684A=
NM_000781.2:c.398A=	NP_000772.2:p.Tyr133=
NM_001099773.1:c.-77A=	NP_001093243.1:n.-77A=
NM_000781.3:c.398A= MANE Select	NP_000772.2:p.Tyr133=
NM_001099773.2:c.-77A=	NP_001093243.1:n.-77A=