Canonical Allele Identifier: CA1328929599
Gene: CYP27A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814183C= , CM000664.2:g.218814183C= GRCh38
NC_000002.11:g.219678906C= , CM000664.1:g.219678906C= GRCh37
NC_000002.10:g.219387150C= NCBI36
NG_007959.1:g.37435C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1180C= MANE Select ENSP00000258415.4:p.Leu394=
ENST00000258415.8:c.1180C= ENSP00000258415.4:p.Leu394=
ENST00000494263.5:n.1614C=
NM_000784.3:c.1180C= NP_000775.1:p.Leu394=
XM_017003488.2:c.760C= XP_016858977.1:p.Leu254=
NM_000784.4:c.1180C= MANE Select NP_000775.1:p.Leu394=