Canonical Allele Identifier: CA2587946778
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525165_7525166insCCATTAT , CM000681.2:g.7525165_7525166insCCATTAT GRCh38
NC_000019.9:g.7590051_7590052insCCATTAT , CM000681.1:g.7590051_7590052insCCATTAT GRCh37
NC_000019.8:g.7496051_7496052insCCATTAT NCBI36
NG_015806.1:g.7556_7557insCCATTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.236_237insCCATTAT MANE Select ENSP00000264079.5:p.Gln79HisfsTer11
ENST00000264079.10:c.236_237insCCATTAT ENSP00000264079.5:p.Gln79HisfsTer11
ENST00000394321.9:n.316_317insCCATTAT
ENST00000596390.1:n.352_353insCCATTAT
ENST00000601003.1:c.236_237insCCATTAT ENSP00000469074.1:p.Gln79HisfsTer11
NM_020533.2:c.236_237insCCATTAT NP_065394.1:p.Gln79HisfsTer11
NM_020533.3:c.236_237insCCATTAT MANE Select NP_065394.1:p.Gln79HisfsTer11