Canonical Allele Identifier: CA2112695
Gene: CYP27A1 HGNC NCBI

Linked Data

dbSNP Id: rs780781879

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218812601del , CM000664.2:g.218812601del GRCh38
NC_000002.11:g.219677324del , CM000664.1:g.219677324del GRCh37
NC_000002.10:g.219385568del NCBI36
NG_007959.1:g.35853del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.696del MANE Select ENSP00000258415.4:p.Ile233SerfsTer6
ENST00000258415.8:c.696del ENSP00000258415.4:p.Ile233SerfsTer6
ENST00000411688.1:c.414del ENSP00000392671.1:p.Ile139SerfsTer6
ENST00000445971.1:c.*157del ENSP00000404945.1:n.*157del
ENST00000466602.1:n.644del
ENST00000494263.5:n.1130del
NM_000784.3:c.696del NP_000775.1:p.Ile233SerfsTer6
XM_017003488.2:c.276del XP_016858977.1:p.Ile93SerfsTer6
NM_000784.4:c.696del MANE Select NP_000775.1:p.Ile233SerfsTer6