Canonical Allele Identifier: CA2573135312
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1418362
ClinVar RCV Id: RCV001952079
dbSNP Id: rs2105980153

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218812607del , CM000664.2:g.218812607del GRCh38
NC_000002.11:g.219677330del , CM000664.1:g.219677330del GRCh37
NC_000002.10:g.219385574del NCBI36
NG_007959.1:g.35859del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.702del MANE Select ENSP00000258415.4:p.Glu235ArgfsTer4
ENST00000258415.8:c.702del ENSP00000258415.4:p.Glu235ArgfsTer4
ENST00000411688.1:c.420del ENSP00000392671.1:p.Glu141ArgfsTer4
ENST00000445971.1:c.*163del ENSP00000404945.1:n.*163del
ENST00000466602.1:n.650del
ENST00000494263.5:n.1136del
NM_000784.3:c.702del NP_000775.1:p.Glu235ArgfsTer4
XM_017003488.2:c.282del XP_016858977.1:p.Glu95ArgfsTer4
NM_000784.4:c.702del MANE Select NP_000775.1:p.Glu235ArgfsTer4