Canonical Allele Identifier: CA1328929538
Gene: CYP27A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814062G= , CM000664.2:g.218814062G= GRCh38
NC_000002.11:g.219678785G= , CM000664.1:g.219678785G= GRCh37
NC_000002.10:g.219387029G= NCBI36
NG_007959.1:g.37314G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1059G= MANE Select ENSP00000258415.4:p.Lys353=
ENST00000258415.8:c.1059G= ENSP00000258415.4:p.Lys353=
ENST00000445971.1:c.*520G= ENSP00000404945.1:n.*520G=
ENST00000466602.1:n.1181G=
ENST00000494263.5:n.1493G=
NM_000784.3:c.1059G= NP_000775.1:p.Lys353=
XM_017003488.2:c.639G= XP_016858977.1:p.Lys213=
NM_000784.4:c.1059G= MANE Select NP_000775.1:p.Lys353=