Canonical Allele Identifier: CA2320962396
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527629G= , CM000681.2:g.7527629G= GRCh38
NC_000019.9:g.7592515G= , CM000681.1:g.7592515G= GRCh37
NC_000019.8:g.7498515G= NCBI36
NG_015806.1:g.10020G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.680+1G= MANE Select ENSP00000264079.5:n.680+1G=
ENST00000264079.10:c.680+1G= ENSP00000264079.5:n.680+1G=
ENST00000394321.9:n.761G=
ENST00000598406.1:n.502G=
ENST00000601003.1:c.572-235G= ENSP00000469074.1:n.572-235G=
NM_020533.2:c.680+1G= NP_065394.1:n.680+1G=
NM_020533.3:c.680+1G= MANE Select NP_065394.1:n.680+1G=