Canonical Allele Identifier: CA1328929534
Gene: CYP27A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814055T= , CM000664.2:g.218814055T= GRCh38
NC_000002.11:g.219678778T= , CM000664.1:g.219678778T= GRCh37
NC_000002.10:g.219387022T= NCBI36
NG_007959.1:g.37307T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1052T= MANE Select ENSP00000258415.4:p.Leu351=
ENST00000258415.8:c.1052T= ENSP00000258415.4:p.Leu351=
ENST00000445971.1:c.*513T= ENSP00000404945.1:n.*513T=
ENST00000466602.1:n.1174T=
ENST00000494263.5:n.1486T=
NM_000784.3:c.1052T= NP_000775.1:p.Leu351=
XM_017003488.2:c.632T= XP_016858977.1:p.Leu211=
NM_000784.4:c.1052T= MANE Select NP_000775.1:p.Leu351=