Canonical Allele Identifier: CA1328929552
Gene: CYP27A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814090G= , CM000664.2:g.218814090G= GRCh38
NC_000002.11:g.219678813G= , CM000664.1:g.219678813G= GRCh37
NC_000002.10:g.219387057G= NCBI36
NG_007959.1:g.37342G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258415.9:c.1087G= MANE Select ENSP00000258415.4:p.Glu363=
ENST00000258415.8:c.1087G= ENSP00000258415.4:p.Glu363=
ENST00000466602.1:n.1209G=
ENST00000494263.5:n.1521G=
NM_000784.3:c.1087G= NP_000775.1:p.Glu363=
XM_017003488.2:c.667G= XP_016858977.1:p.Glu223=
NM_000784.4:c.1087G= MANE Select NP_000775.1:p.Glu363=