Canonical Allele Identifier: CA2320962005
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526859G= , CM000681.2:g.7526859G= GRCh38
NC_000019.9:g.7591745G= , CM000681.1:g.7591745G= GRCh37
NC_000019.8:g.7497745G= NCBI36
NG_015806.1:g.9250G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.504G= MANE Select ENSP00000264079.5:p.Arg168=
ENST00000264079.10:c.504G= ENSP00000264079.5:p.Arg168=
ENST00000394321.9:n.584G=
ENST00000596008.1:n.466G=
ENST00000598406.1:n.325G=
ENST00000601003.1:c.504G= ENSP00000469074.1:p.Arg168=
NM_020533.2:c.504G= NP_065394.1:p.Arg168=
NM_020533.3:c.504G= MANE Select NP_065394.1:p.Arg168=