Canonical Allele Identifier: CA491194342

Gene: CYP11A1

Linked Data

• MyVariant Identifiers: chr15:g.74631978C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339637C>G , CM000677.2:g.74339637C>G	GRCh38
NC_000015.9:g.74631978C>G , CM000677.1:g.74631978C>G	GRCh37
NC_000015.8:g.72419031C>G	NCBI36
NG_007973.1:g.33105G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.1107G>C MANE Select	ENSP00000268053.6:p.Thr369=
ENST00000268053.10:c.1107G>C	ENSP00000268053.6:p.Thr369=
ENST00000358632.8:c.633G>C	ENSP00000351455.4:p.Thr211=
ENST00000435365.5:c.1107G>C	ENSP00000391081.1:p.Thr369=
ENST00000566674.5:c.633G>C	ENSP00000456941.1:p.Thr211=
NM_000781.2:c.1107G>C	NP_000772.2:p.Thr369=
NM_001099773.1:c.633G>C	NP_001093243.1:p.Thr211=
NM_000781.3:c.1107G>C MANE Select	NP_000772.2:p.Thr369=
NM_001099773.2:c.633G>C	NP_001093243.1:p.Thr211=