Canonical Allele Identifier: CA2739272098
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2830348
ClinVar RCV Id: RCV003694173

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764107del , CM000674.2:g.57764107del GRCh38
NC_000012.11:g.58157890del , CM000674.1:g.58157890del GRCh37
NC_000012.10:g.56444157del NCBI36
NG_007076.1:g.8090del

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1290del ENSP00000518840.1:p.Asn432IlefsTer?
ENST00000713545.1:c.*214del ENSP00000518841.1:n.*214del
ENST00000228606.9:c.1209del MANE Select ENSP00000228606.4:p.Asn405IlefsTer?
ENST00000228606.8:c.1209del ENSP00000228606.4:p.Asn405IlefsTer?
ENST00000547344.5:n.1348del
NM_000785.3:c.1209del NP_000776.1:p.Asn405IlefsTer?
NM_000785.4:c.1209del MANE Select NP_000776.1:p.Asn405IlefsTer?