Canonical Allele Identifier: CA491194274

Gene: CYP11A1

Linked Data

• MyVariant Identifiers: chr15:g.74631954G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339613G>A , CM000677.2:g.74339613G>A	GRCh38
NC_000015.9:g.74631954G>A , CM000677.1:g.74631954G>A	GRCh37
NC_000015.8:g.72419007G>A	NCBI36
NG_007973.1:g.33129C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.1131C>T MANE Select	ENSP00000268053.6:p.Leu377=
ENST00000268053.10:c.1131C>T	ENSP00000268053.6:p.Leu377=
ENST00000358632.8:c.657C>T	ENSP00000351455.4:p.Leu219=
ENST00000435365.5:c.1131C>T	ENSP00000391081.1:p.Leu377=
ENST00000566674.5:c.657C>T	ENSP00000456941.1:p.Leu219=
NM_000781.2:c.1131C>T	NP_000772.2:p.Leu377=
NM_001099773.1:c.657C>T	NP_001093243.1:p.Leu219=
NM_000781.3:c.1131C>T MANE Select	NP_000772.2:p.Leu377=
NM_001099773.2:c.657C>T	NP_001093243.1:p.Leu219=