Canonical Allele Identifier: CA491194446

Gene: CYP11A1

Linked Data

• MyVariant Identifiers: chr15:g.74632083G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339742G>T , CM000677.2:g.74339742G>T	GRCh38
NC_000015.9:g.74632083G>T , CM000677.1:g.74632083G>T	GRCh37
NC_000015.8:g.72419136G>T	NCBI36
NG_007973.1:g.33000C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.1002C>A MANE Select	ENSP00000268053.6:p.Thr334=
ENST00000268053.10:c.1002C>A	ENSP00000268053.6:p.Thr334=
ENST00000358632.8:c.528C>A	ENSP00000351455.4:p.Thr176=
ENST00000435365.5:c.1002C>A	ENSP00000391081.1:p.Thr334=
ENST00000566674.5:c.528C>A	ENSP00000456941.1:p.Thr176=
NM_000781.2:c.1002C>A	NP_000772.2:p.Thr334=
NM_001099773.1:c.528C>A	NP_001093243.1:p.Thr176=
NM_000781.3:c.1002C>A MANE Select	NP_000772.2:p.Thr334=
NM_001099773.2:c.528C>A	NP_001093243.1:p.Thr176=