Canonical Allele Identifier: CA2320962706
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528238C= , CM000681.2:g.7528238C= GRCh38
NC_000019.9:g.7593124C= , CM000681.1:g.7593124C= GRCh37
NC_000019.8:g.7499124C= NCBI36
NG_015806.1:g.10629C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.858C= MANE Select ENSP00000264079.5:p.His286=
ENST00000264079.10:c.858C= ENSP00000264079.5:p.His286=
ENST00000394321.9:n.1173C=
NM_020533.2:c.858C= NP_065394.1:p.His286=
NM_020533.3:c.858C= MANE Select NP_065394.1:p.His286=