Canonical Allele Identifier: CA2739638001
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527853C>G , CM000681.2:g.7527853C>G GRCh38
NC_000019.9:g.7592739C>G , CM000681.1:g.7592739C>G GRCh37
NC_000019.8:g.7498739C>G NCBI36
NG_015806.1:g.10244C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-11C>G MANE Select ENSP00000264079.5:n.681-11C>G
ENST00000264079.10:c.681-11C>G ENSP00000264079.5:n.681-11C>G
ENST00000394321.9:n.985C>G
ENST00000601003.1:c.572-11C>G ENSP00000469074.1:n.572-11C>G
NM_020533.2:c.681-11C>G NP_065394.1:n.681-11C>G
NM_020533.3:c.681-11C>G MANE Select NP_065394.1:n.681-11C>G