Canonical Allele Identifier: CA393150249
Gene: CYP11A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74347952G>C , CM000677.2:g.74347952G>C GRCh38
NC_000015.9:g.74640293G>C , CM000677.1:g.74640293G>C GRCh37
NC_000015.8:g.72427346G>C NCBI36
NG_007973.1:g.24790C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000268053.11:c.373C>G MANE Select ENSP00000268053.6:p.Pro125Ala
ENST00000268053.10:c.373C>G ENSP00000268053.6:p.Pro125Ala
ENST00000358632.8:c.-102C>G ENSP00000351455.4:n.-102C>G
ENST00000416978.1:c.373C>G ENSP00000388018.1:p.Pro125Ala
ENST00000435365.5:c.373C>G ENSP00000391081.1:p.Pro125Ala
ENST00000450547.1:c.-102C>G ENSP00000402064.1:n.-102C>G
ENST00000466978.1:n.767C>G
ENST00000566674.5:c.-102C>G ENSP00000456941.1:n.-102C>G
ENST00000569662.1:c.-49-2709C>G ENSP00000456598.1:n.-49-2709C>G
NM_000781.2:c.373C>G NP_000772.2:p.Pro125Ala
NM_001099773.1:c.-102C>G NP_001093243.1:n.-102C>G
NM_000781.3:c.373C>G MANE Select NP_000772.2:p.Pro125Ala
NM_001099773.2:c.-102C>G NP_001093243.1:n.-102C>G