Canonical Allele Identifier: CA2580097121
Gene: MCOLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1726055
ClinVar RCV Id: RCV002307026

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528245_7528246insACTG , CM000681.2:g.7528245_7528246insACTG GRCh38
NC_000019.9:g.7593131_7593132insACTG , CM000681.1:g.7593131_7593132insACTG GRCh37
NC_000019.8:g.7499131_7499132insACTG NCBI36
NG_015806.1:g.10636_10637insACTG

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.865_866insACTG MANE Select ENSP00000264079.5:p.Val289AspfsTer15
ENST00000264079.10:c.865_866insACTG ENSP00000264079.5:p.Val289AspfsTer15
ENST00000394321.9:n.1180_1181insACTG
NM_020533.2:c.865_866insACTG NP_065394.1:p.Val289AspfsTer15
NM_020533.3:c.865_866insACTG MANE Select NP_065394.1:p.Val289AspfsTer15