Canonical Allele Identifier: CA1328929598
Gene: CYP27A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814180A= , CM000664.2:g.218814180A= GRCh38
NC_000002.11:g.219678903A= , CM000664.1:g.219678903A= GRCh37
NC_000002.10:g.219387147A= NCBI36
NG_007959.1:g.37432A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1177A= MANE Select ENSP00000258415.4:p.Thr393=
ENST00000258415.8:c.1177A= ENSP00000258415.4:p.Thr393=
ENST00000494263.5:n.1611A=
NM_000784.3:c.1177A= NP_000775.1:p.Thr393=
XM_017003488.2:c.757A= XP_016858977.1:p.Thr253=
NM_000784.4:c.1177A= MANE Select NP_000775.1:p.Thr393=