Canonical Allele Identifier: CA2576596962
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527470G>C , CM000681.2:g.7527470G>C GRCh38
NC_000019.9:g.7592356G>C , CM000681.1:g.7592356G>C GRCh37
NC_000019.8:g.7498356G>C NCBI36
NG_015806.1:g.9861G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.572-50G>C MANE Select ENSP00000264079.5:n.572-50G>C
ENST00000264079.10:c.572-50G>C ENSP00000264079.5:n.572-50G>C
ENST00000394321.9:n.652-50G>C
ENST00000598406.1:n.393-50G>C
ENST00000601003.1:c.572-394G>C ENSP00000469074.1:n.572-394G>C
NM_020533.2:c.572-50G>C NP_065394.1:n.572-50G>C
NM_020533.3:c.572-50G>C MANE Select NP_065394.1:n.572-50G>C