Canonical Allele Identifier: CA2320961891
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526659A= , CM000681.2:g.7526659A= GRCh38
NC_000019.9:g.7591545A= , CM000681.1:g.7591545A= GRCh37
NC_000019.8:g.7497545A= NCBI36
NG_015806.1:g.9050A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.405+53A= MANE Select ENSP00000264079.5:n.405+53A=
ENST00000264079.10:c.405+53A= ENSP00000264079.5:n.405+53A=
ENST00000394321.9:n.485+53A=
ENST00000596008.1:n.367+53A=
ENST00000598406.1:n.226+53A=
ENST00000601003.1:c.405+53A= ENSP00000469074.1:n.405+53A=
NM_020533.2:c.405+53A= NP_065394.1:n.405+53A=
NM_020533.3:c.405+53A= MANE Select NP_065394.1:n.405+53A=