Canonical Allele Identifier: CA393147128
Gene: CYP11A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74339678C>A , CM000677.2:g.74339678C>A GRCh38
NC_000015.9:g.74632019C>A , CM000677.1:g.74632019C>A GRCh37
NC_000015.8:g.72419072C>A NCBI36
NG_007973.1:g.33064G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000268053.11:c.1066G>T MANE Select ENSP00000268053.6:p.Val356Phe
ENST00000268053.10:c.1066G>T ENSP00000268053.6:p.Val356Phe
ENST00000358632.8:c.592G>T ENSP00000351455.4:p.Val198Phe
ENST00000435365.5:c.1066G>T ENSP00000391081.1:p.Val356Phe
ENST00000566674.5:c.592G>T ENSP00000456941.1:p.Val198Phe
NM_000781.2:c.1066G>T NP_000772.2:p.Val356Phe
NM_001099773.1:c.592G>T NP_001093243.1:p.Val198Phe
NM_000781.3:c.1066G>T MANE Select NP_000772.2:p.Val356Phe
NM_001099773.2:c.592G>T NP_001093243.1:p.Val198Phe