Canonical Allele Identifier: CA1328928796
Gene: CYP27A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218812508T= , CM000664.2:g.218812508T= GRCh38
NC_000002.11:g.219677231T= , CM000664.1:g.219677231T= GRCh37
NC_000002.10:g.219385475T= NCBI36
NG_007959.1:g.35760T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.647-44T= MANE Select ENSP00000258415.4:n.647-44T=
ENST00000258415.8:c.647-44T= ENSP00000258415.4:n.647-44T=
ENST00000411688.1:c.365-44T= ENSP00000392671.1:n.365-44T=
ENST00000445971.1:c.*108-44T= ENSP00000404945.1:n.*108-44T=
ENST00000466602.1:n.551T=
ENST00000494263.5:n.1081-44T=
NM_000784.3:c.647-44T= NP_000775.1:n.647-44T=
XM_017003488.2:c.227-44T= XP_016858977.1:n.227-44T=
NM_000784.4:c.647-44T= MANE Select NP_000775.1:n.647-44T=