Canonical Allele Identifier: CA403084884
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.857A>C MANE Select ENSP00000264079.5:p.His286Pro
ENST00000264079.10:c.857A>C ENSP00000264079.5:p.His286Pro
ENST00000394321.9:n.1172A>C
NM_020533.2:c.857A>C NP_065394.1:p.His286Pro
NM_020533.3:c.857A>C MANE Select NP_065394.1:p.His286Pro