Canonical Allele Identifier: CA491194260
Gene: CYP11A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.74631948G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74339607G>C , CM000677.2:g.74339607G>C GRCh38
NC_000015.9:g.74631948G>C , CM000677.1:g.74631948G>C GRCh37
NC_000015.8:g.72419001G>C NCBI36
NG_007973.1:g.33135C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000268053.11:c.1137C>G MANE Select ENSP00000268053.6:p.Ala379=
ENST00000268053.10:c.1137C>G ENSP00000268053.6:p.Ala379=
ENST00000358632.8:c.663C>G ENSP00000351455.4:p.Ala221=
ENST00000435365.5:c.1137C>G ENSP00000391081.1:p.Ala379=
ENST00000566674.5:c.663C>G ENSP00000456941.1:p.Ala221=
NM_000781.2:c.1137C>G NP_000772.2:p.Ala379=
NM_001099773.1:c.663C>G NP_001093243.1:p.Ala221=
NM_000781.3:c.1137C>G MANE Select NP_000772.2:p.Ala379=
NM_001099773.2:c.663C>G NP_001093243.1:p.Ala221=