Canonical Allele Identifier: CA2187637871

Gene: CYP11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339583T= , CM000677.2:g.74339583T=	GRCh38
NC_000015.9:g.74631924T= , CM000677.1:g.74631924T=	GRCh37
NC_000015.8:g.72418977T=	NCBI36
NG_007973.1:g.33159A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000268053.11:c.1157+4A= MANE Select	ENSP00000268053.6:n.1157+4A=
ENST00000268053.10:c.1157+4A=	ENSP00000268053.6:n.1157+4A=
ENST00000358632.8:c.683+4A=	ENSP00000351455.4:n.683+4A=
ENST00000435365.5:c.1157+4A=	ENSP00000391081.1:n.1157+4A=
NM_000781.2:c.1157+4A=	NP_000772.2:n.1157+4A=
NM_001099773.1:c.683+4A=	NP_001093243.1:n.683+4A=
NM_000781.3:c.1157+4A= MANE Select	NP_000772.2:n.1157+4A=
NM_001099773.2:c.683+4A=	NP_001093243.1:n.683+4A=