Canonical Allele Identifier: CA2663168095
Gene: CYP27A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814213dup , CM000664.2:g.218814213dup GRCh38
NC_000002.11:g.219678936dup , CM000664.1:g.219678936dup GRCh37
NC_000002.10:g.219387180dup NCBI36
NG_007959.1:g.37465dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1184+26dup MANE Select ENSP00000258415.4:n.1184+26dup
ENST00000258415.8:c.1184+26dup ENSP00000258415.4:n.1184+26dup
ENST00000494263.5:n.1644dup
NM_000784.3:c.1184+26dup NP_000775.1:n.1184+26dup
XM_017003488.2:c.764+26dup XP_016858977.1:n.764+26dup
NM_000784.4:c.1184+26dup MANE Select NP_000775.1:n.1184+26dup