Canonical Allele Identifier: CA2320961148
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525148C= , CM000681.2:g.7525148C= GRCh38
NC_000019.9:g.7590034C= , CM000681.1:g.7590034C= GRCh37
NC_000019.8:g.7496034C= NCBI36
NG_015806.1:g.7539C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.219C= MANE Select ENSP00000264079.5:p.Ile73=
ENST00000264079.10:c.219C= ENSP00000264079.5:p.Ile73=
ENST00000394321.9:n.299C=
ENST00000596390.1:n.335C=
ENST00000601003.1:c.219C= ENSP00000469074.1:p.Ile73=
NM_020533.2:c.219C= NP_065394.1:p.Ile73=
NM_020533.3:c.219C= MANE Select NP_065394.1:p.Ile73=