Canonical Allele Identifier: CA403084886
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528237A>G , CM000681.2:g.7528237A>G GRCh38
NC_000019.9:g.7593123A>G , CM000681.1:g.7593123A>G GRCh37
NC_000019.8:g.7499123A>G NCBI36
NG_015806.1:g.10628A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.857A>G MANE Select ENSP00000264079.5:p.His286Arg
ENST00000264079.10:c.857A>G ENSP00000264079.5:p.His286Arg
ENST00000394321.9:n.1172A>G
NM_020533.2:c.857A>G NP_065394.1:p.His286Arg
NM_020533.3:c.857A>G MANE Select NP_065394.1:p.His286Arg