Canonical Allele Identifier: CA272794689

Gene: CYP11A1

Linked Data

• dbSNP Id: rs764293251
• gnomAD v3: 15-74345432-G-A
• gnomAD v4: 15-74345432-G-A
• MyVariant Identifiers: chr15:g.74637773G>A (hg19) ; chr15:g.74345432G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74345432G>A , CM000677.2:g.74345432G>A	GRCh38
NC_000015.9:g.74637773G>A , CM000677.1:g.74637773G>A	GRCh37
NC_000015.8:g.72424826G>A	NCBI36
NG_007973.1:g.27310C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.426-189C>T MANE Select	ENSP00000268053.6:n.426-189C>T
ENST00000268053.10:c.426-189C>T	ENSP00000268053.6:n.426-189C>T
ENST00000358632.8:c.-49-189C>T	ENSP00000351455.4:n.-49-189C>T
ENST00000416978.1:c.426-142C>T	ENSP00000388018.1:n.426-142C>T
ENST00000435365.5:c.426-189C>T	ENSP00000391081.1:n.426-189C>T
ENST00000450547.1:c.-49-189C>T	ENSP00000402064.1:n.-49-189C>T
ENST00000466978.1:n.820-189C>T
ENST00000566674.5:c.-49-189C>T	ENSP00000456941.1:n.-49-189C>T
ENST00000569662.1:c.-49-189C>T	ENSP00000456598.1:n.-49-189C>T
NM_000781.2:c.426-189C>T	NP_000772.2:n.426-189C>T
NM_001099773.1:c.-49-189C>T	NP_001093243.1:n.-49-189C>T
NM_000781.3:c.426-189C>T MANE Select	NP_000772.2:n.426-189C>T
NM_001099773.2:c.-49-189C>T	NP_001093243.1:n.-49-189C>T