Canonical Allele Identifier: CA2587950473
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533963del , CM000681.2:g.7533963del GRCh38
NC_000019.9:g.7598849del , CM000681.1:g.7598849del GRCh37
NC_000019.8:g.7504849del NCBI36
NG_013374.1:g.4812del
NG_015806.1:g.16354del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*168del MANE Select ENSP00000264079.5:n.*168del
ENST00000264079.10:c.*168del ENSP00000264079.5:n.*168del
ENST00000394321.9:n.2226del
ENST00000599334.1:c.639del
ENST00000601870.1:c.169+95del
ENST00000602227.1:n.465del
NM_020533.2:c.*168del NP_065394.1:n.*168del
NM_020533.3:c.*168del MANE Select NP_065394.1:n.*168del