Canonical Allele Identifier: CA9138782
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs199879376
gnomAD v2: 19-7592374-C-T
gnomAD v4: 19-7527488-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527488C>T , CM000681.2:g.7527488C>T GRCh38
NC_000019.9:g.7592374C>T , CM000681.1:g.7592374C>T GRCh37
NC_000019.8:g.7498374C>T NCBI36
NG_015806.1:g.9879C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.572-32C>T MANE Select ENSP00000264079.5:n.572-32C>T
ENST00000264079.10:c.572-32C>T ENSP00000264079.5:n.572-32C>T
ENST00000394321.9:n.652-32C>T
ENST00000598406.1:n.393-32C>T
ENST00000601003.1:c.572-376C>T ENSP00000469074.1:n.572-376C>T
NM_020533.2:c.572-32C>T NP_065394.1:n.572-32C>T
NM_020533.3:c.572-32C>T MANE Select NP_065394.1:n.572-32C>T