Canonical Allele Identifier: CA393147152

Gene: CYP11A1

Linked Data

• MyVariant Identifiers: chr15:g.74632032C>A (hg19) ; chr15:g.74339691C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74339691C>A , CM000677.2:g.74339691C>A	GRCh38
NC_000015.9:g.74632032C>A , CM000677.1:g.74632032C>A	GRCh37
NC_000015.8:g.72419085C>A	NCBI36
NG_007973.1:g.33051G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268053.11:c.1053G>T MANE Select	ENSP00000268053.6:p.Met351Ile
ENST00000268053.10:c.1053G>T	ENSP00000268053.6:p.Met351Ile
ENST00000358632.8:c.579G>T	ENSP00000351455.4:p.Met193Ile
ENST00000435365.5:c.1053G>T	ENSP00000391081.1:p.Met351Ile
ENST00000566674.5:c.579G>T	ENSP00000456941.1:p.Met193Ile
NM_000781.2:c.1053G>T	NP_000772.2:p.Met351Ile
NM_001099773.1:c.579G>T	NP_001093243.1:p.Met193Ile
NM_000781.3:c.1053G>T MANE Select	NP_000772.2:p.Met351Ile
NM_001099773.2:c.579G>T	NP_001093243.1:p.Met193Ile