Canonical Allele Identifier: CA2320961131
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7524980C= , CM000681.2:g.7524980C= GRCh38
NC_000019.9:g.7589866C= , CM000681.1:g.7589866C= GRCh37
NC_000019.8:g.7495866C= NCBI36
NG_015806.1:g.7371C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.51C= MANE Select ENSP00000264079.5:p.Thr17=
ENST00000264079.10:c.51C= ENSP00000264079.5:p.Thr17=
ENST00000394321.9:n.131C=
ENST00000596390.1:n.167C=
ENST00000601003.1:c.51C= ENSP00000469074.1:p.Thr17=
NM_020533.2:c.51C= NP_065394.1:p.Thr17=
XR_936293.2:n.1G=
XR_936294.2:n.1G=
NM_020533.3:c.51C= MANE Select NP_065394.1:p.Thr17=