Canonical Allele Identifier: CA1328929539
Gene: CYP27A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814064A= , CM000664.2:g.218814064A= GRCh38
NC_000002.11:g.219678787A= , CM000664.1:g.219678787A= GRCh37
NC_000002.10:g.219387031A= NCBI36
NG_007959.1:g.37316A=

Transcript Alleles

HGVS Amino-acid change
ENST00000258415.9:c.1061A= MANE Select ENSP00000258415.4:p.Asp354=
ENST00000258415.8:c.1061A= ENSP00000258415.4:p.Asp354=
ENST00000445971.1:c.*522A= ENSP00000404945.1:n.*522A=
ENST00000466602.1:n.1183A=
ENST00000494263.5:n.1495A=
NM_000784.3:c.1061A= NP_000775.1:p.Asp354=
XM_017003488.2:c.641A= XP_016858977.1:p.Asp214=
NM_000784.4:c.1061A= MANE Select NP_000775.1:p.Asp354=