Canonical Allele Identifier: CA1328929609
Gene: CYP27A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814201C= , CM000664.2:g.218814201C= GRCh38
NC_000002.11:g.219678924C= , CM000664.1:g.219678924C= GRCh37
NC_000002.10:g.219387168C= NCBI36
NG_007959.1:g.37453C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258415.9:c.1184+14C= MANE Select ENSP00000258415.4:n.1184+14C=
ENST00000258415.8:c.1184+14C= ENSP00000258415.4:n.1184+14C=
ENST00000494263.5:n.1632C=
NM_000784.3:c.1184+14C= NP_000775.1:n.1184+14C=
XM_017003488.2:c.764+14C= XP_016858977.1:n.764+14C=
NM_000784.4:c.1184+14C= MANE Select NP_000775.1:n.1184+14C=
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