Canonical Allele Identifier: CA2629471165

Gene: CYP11A1

Linked Data

• gnomAD v4: 15-74347750-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74347750A>G , CM000677.2:g.74347750A>G	GRCh38
NC_000015.9:g.74640091A>G , CM000677.1:g.74640091A>G	GRCh37
NC_000015.8:g.72427144A>G	NCBI36
NG_007973.1:g.24992T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.425+150T>C MANE Select	ENSP00000268053.6:n.425+150T>C
ENST00000268053.10:c.425+150T>C	ENSP00000268053.6:n.425+150T>C
ENST00000358632.8:c.-50+150T>C	ENSP00000351455.4:n.-50+150T>C
ENST00000416978.1:c.425+150T>C	ENSP00000388018.1:n.425+150T>C
ENST00000435365.5:c.425+150T>C	ENSP00000391081.1:n.425+150T>C
ENST00000450547.1:c.-50+150T>C	ENSP00000402064.1:n.-50+150T>C
ENST00000466978.1:n.819+150T>C
ENST00000566674.5:c.-50+150T>C	ENSP00000456941.1:n.-50+150T>C
ENST00000569662.1:c.-49-2507T>C	ENSP00000456598.1:n.-49-2507T>C
NM_000781.2:c.425+150T>C	NP_000772.2:n.425+150T>C
NM_001099773.1:c.-50+150T>C	NP_001093243.1:n.-50+150T>C
NM_000781.3:c.425+150T>C MANE Select	NP_000772.2:n.425+150T>C
NM_001099773.2:c.-50+150T>C	NP_001093243.1:n.-50+150T>C