Canonical Allele Identifier: CA2187642638

Gene: CYP11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74345451_74345453delinsAAG , CM000677.2:g.74345451_74345453delinsAAG	GRCh38
NC_000015.9:g.74637792_74637794delinsAAG , CM000677.1:g.74637792_74637794delinsAAG	GRCh37
NC_000015.8:g.72424845_72424847delinsAAG	NCBI36
NG_007973.1:g.27289_27291delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.426-210_426-208delinsCTT MANE Select	ENSP00000268053.6:n.426-210_426-208delinsCTT
ENST00000268053.10:c.426-210_426-208delinsCTT	ENSP00000268053.6:n.426-210_426-208delinsCTT
ENST00000358632.8:c.-49-210_-49-208delinsCTT	ENSP00000351455.4:n.-49-210_-49-208delinsCTT
ENST00000416978.1:c.426-163_426-161delinsCTT	ENSP00000388018.1:n.426-163_426-161delinsCTT
ENST00000435365.5:c.426-210_426-208delinsCTT	ENSP00000391081.1:n.426-210_426-208delinsCTT
ENST00000450547.1:c.-49-210_-49-208delinsCTT	ENSP00000402064.1:n.-49-210_-49-208delinsCTT
ENST00000466978.1:n.820-210_820-208delinsCTT
ENST00000566674.5:c.-49-210_-49-208delinsCTT	ENSP00000456941.1:n.-49-210_-49-208delinsCTT
ENST00000569662.1:c.-49-210_-49-208delinsCTT	ENSP00000456598.1:n.-49-210_-49-208delinsCTT
NM_000781.2:c.426-210_426-208delinsCTT	NP_000772.2:n.426-210_426-208delinsCTT
NM_001099773.1:c.-49-210_-49-208delinsCTT	NP_001093243.1:n.-49-210_-49-208delinsCTT
NM_000781.3:c.426-210_426-208delinsCTT MANE Select	NP_000772.2:n.426-210_426-208delinsCTT
NM_001099773.2:c.-49-210_-49-208delinsCTT	NP_001093243.1:n.-49-210_-49-208delinsCTT