Canonical Allele Identifier: CA491194448

Gene: CYP11A1

Linked Data

• MyVariant Identifiers: chr15:g.74632089G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339748G>C , CM000677.2:g.74339748G>C	GRCh38
NC_000015.9:g.74632089G>C , CM000677.1:g.74632089G>C	GRCh37
NC_000015.8:g.72419142G>C	NCBI36
NG_007973.1:g.32994C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.996C>G MANE Select	ENSP00000268053.6:p.Ser332=
ENST00000268053.10:c.996C>G	ENSP00000268053.6:p.Ser332=
ENST00000358632.8:c.522C>G	ENSP00000351455.4:p.Ser174=
ENST00000435365.5:c.996C>G	ENSP00000391081.1:p.Ser332=
ENST00000566674.5:c.522C>G	ENSP00000456941.1:p.Ser174=
NM_000781.2:c.996C>G	NP_000772.2:p.Ser332=
NM_001099773.1:c.522C>G	NP_001093243.1:p.Ser174=
NM_000781.3:c.996C>G MANE Select	NP_000772.2:p.Ser332=
NM_001099773.2:c.522C>G	NP_001093243.1:p.Ser174=