Canonical Allele Identifier: CA403084891
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.858C>A MANE Select ENSP00000264079.5:p.His286Gln
ENST00000264079.10:c.858C>A ENSP00000264079.5:p.His286Gln
ENST00000394321.9:n.1173C>A
NM_020533.2:c.858C>A NP_065394.1:p.His286Gln
NM_020533.3:c.858C>A MANE Select NP_065394.1:p.His286Gln