Canonical Allele Identifier: CA1328929586
Gene: CYP27A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814155G= , CM000664.2:g.218814155G= GRCh38
NC_000002.11:g.219678878G= , CM000664.1:g.219678878G= GRCh37
NC_000002.10:g.219387122G= NCBI36
NG_007959.1:g.37407G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1152G= MANE Select ENSP00000258415.4:p.Pro384=
ENST00000258415.8:c.1152G= ENSP00000258415.4:p.Pro384=
ENST00000494263.5:n.1586G=
NM_000784.3:c.1152G= NP_000775.1:p.Pro384=
XM_017003488.2:c.732G= XP_016858977.1:p.Pro244=
NM_000784.4:c.1152G= MANE Select NP_000775.1:p.Pro384=
Search 100 bp 5'
Search 100 bp 3'