Canonical Allele Identifier: CA1328928979
Gene: CYP27A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218812857T= , CM000664.2:g.218812857T= GRCh38
NC_000002.11:g.219677580T= , CM000664.1:g.219677580T= GRCh37
NC_000002.10:g.219385824T= NCBI36
NG_007959.1:g.36109T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.845-67T= MANE Select ENSP00000258415.4:n.845-67T=
ENST00000258415.8:c.845-67T= ENSP00000258415.4:n.845-67T=
ENST00000411688.1:c.563-67T= ENSP00000392671.1:n.563-67T=
ENST00000445971.1:c.*306-67T= ENSP00000404945.1:n.*306-67T=
ENST00000466602.1:n.900T=
ENST00000494263.5:n.1279-67T=
NM_000784.3:c.845-67T= NP_000775.1:n.845-67T=
XM_017003488.2:c.425-67T= XP_016858977.1:n.425-67T=
NM_000784.4:c.845-67T= MANE Select NP_000775.1:n.845-67T=
Search 100 bp 5'
Search 100 bp 3'