Canonical Allele Identifier: CA350591519
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 597716
dbSNP Id: rs780927834

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814058C>T , CM000664.2:g.218814058C>T GRCh38
NC_000002.11:g.219678781C>T , CM000664.1:g.219678781C>T GRCh37
NC_000002.10:g.219387025C>T NCBI36
NG_007959.1:g.37310C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1055C>T MANE Select ENSP00000258415.4:p.Ser352Leu
ENST00000258415.8:c.1055C>T ENSP00000258415.4:p.Ser352Leu
ENST00000445971.1:c.*516C>T ENSP00000404945.1:n.*516C>T
ENST00000466602.1:n.1177C>T
ENST00000494263.5:n.1489C>T
NM_000784.3:c.1055C>T NP_000775.1:p.Ser352Leu
XM_017003488.2:c.635C>T XP_016858977.1:p.Ser212Leu
NM_000784.4:c.1055C>T MANE Select NP_000775.1:p.Ser352Leu