Canonical Allele Identifier: CA2320962508
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527798C= , CM000681.2:g.7527798C= GRCh38
NC_000019.9:g.7592684C= , CM000681.1:g.7592684C= GRCh37
NC_000019.8:g.7498684C= NCBI36
NG_015806.1:g.10189C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-66C= MANE Select ENSP00000264079.5:n.681-66C=
ENST00000264079.10:c.681-66C= ENSP00000264079.5:n.681-66C=
ENST00000394321.9:n.930C=
ENST00000601003.1:c.572-66C= ENSP00000469074.1:n.572-66C=
NM_020533.2:c.681-66C= NP_065394.1:n.681-66C=
NM_020533.3:c.681-66C= MANE Select NP_065394.1:n.681-66C=