Canonical Allele Identifier: CA2587950392
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533845del , CM000681.2:g.7533845del GRCh38
NC_000019.9:g.7598731del , CM000681.1:g.7598731del GRCh37
NC_000019.8:g.7504731del NCBI36
NG_013374.1:g.4694del
NG_015806.1:g.16236del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*50del MANE Select ENSP00000264079.5:n.*50del
ENST00000264079.10:c.*50del ENSP00000264079.5:n.*50del
ENST00000394321.9:n.2108del
ENST00000599334.1:c.521del
ENST00000601870.1:c.146del
ENST00000602227.1:n.347del
NM_020533.2:c.*50del NP_065394.1:n.*50del
NM_020533.3:c.*50del MANE Select NP_065394.1:n.*50del