Canonical Allele Identifier: CA2573148891
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1387998
ClinVar RCV Id: RCV001875717
dbSNP Id: rs2140396403

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764145_57764149dup , CM000674.2:g.57764145_57764149dup GRCh38
NC_000012.11:g.58157928_58157932dup , CM000674.1:g.58157928_58157932dup GRCh37
NC_000012.10:g.56444195_56444199dup NCBI36
NG_007076.1:g.8047_8051dup

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1247_1251dup ENSP00000518840.1:p.Pro418ValfsTer?
ENST00000713545.1:c.*171_*175dup ENSP00000518841.1:n.*171_*175dup
ENST00000228606.9:c.1166_1170dup MANE Select ENSP00000228606.4:p.Pro391ValfsTer?
ENST00000228606.8:c.1166_1170dup ENSP00000228606.4:p.Pro391ValfsTer?
ENST00000546567.5:c.461_465dup ENSP00000449472.1:p.Pro156ValfsTer?
ENST00000547344.5:n.1305_1309dup
NM_000785.3:c.1166_1170dup NP_000776.1:p.Pro391ValfsTer?
NM_000785.4:c.1166_1170dup MANE Select NP_000776.1:p.Pro391ValfsTer?