Canonical Allele Identifier: CA2839076984
Gene: CYP27A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218812527G>T , CM000664.2:g.218812527G>T GRCh38
NC_000002.11:g.219677250G>T , CM000664.1:g.219677250G>T GRCh37
NC_000002.10:g.219385494G>T NCBI36
NG_007959.1:g.35779G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.647-25G>T MANE Select ENSP00000258415.4:n.647-25G>T
ENST00000258415.8:c.647-25G>T ENSP00000258415.4:n.647-25G>T
ENST00000411688.1:c.365-25G>T ENSP00000392671.1:n.365-25G>T
ENST00000445971.1:c.*108-25G>T ENSP00000404945.1:n.*108-25G>T
ENST00000466602.1:n.570G>T
ENST00000494263.5:n.1081-25G>T
NM_000784.3:c.647-25G>T NP_000775.1:n.647-25G>T
XM_017003488.2:c.227-25G>T XP_016858977.1:n.227-25G>T
NM_000784.4:c.647-25G>T MANE Select NP_000775.1:n.647-25G>T