Canonical Allele Identifier: CA2320962514
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527807T= , CM000681.2:g.7527807T= GRCh38
NC_000019.9:g.7592693T= , CM000681.1:g.7592693T= GRCh37
NC_000019.8:g.7498693T= NCBI36
NG_015806.1:g.10198T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-57T= MANE Select ENSP00000264079.5:n.681-57T=
ENST00000264079.10:c.681-57T= ENSP00000264079.5:n.681-57T=
ENST00000394321.9:n.939T=
ENST00000601003.1:c.572-57T= ENSP00000469074.1:n.572-57T=
NM_020533.2:c.681-57T= NP_065394.1:n.681-57T=
NM_020533.3:c.681-57T= MANE Select NP_065394.1:n.681-57T=