Canonical Allele Identifier: CA1328929949
Gene: CYP27A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814912_218814943delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG , CM000664.2:g.218814912_218814943delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG GRCh38
NC_000002.11:g.219679635_219679666delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG , CM000664.1:g.219679635_219679666delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG GRCh37
NC_000002.10:g.219387879_219387910delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG NCBI36
NG_007959.1:g.38164_38195delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1478_1509delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG MANE Select ENSP00000258415.4:p.Leu493=
ENST00000258415.8:c.1478_1509delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG ENSP00000258415.4:p.Leu493=
ENST00000494263.5:n.2190_2221delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG
NM_000784.3:c.1478_1509delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG NP_000775.1:p.Leu493=
XM_017003488.2:c.1058_1089delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG XP_016858977.1:p.Leu353=
NM_000784.4:c.1478_1509delinsTGATCCAGAAGTACAAGGTGGTCCTGGCCCCG MANE Select NP_000775.1:p.Leu493=