Canonical Allele Identifier: CA9138808
Gene: MCOLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1588775
ClinVar RCV Id: RCV002098459
dbSNP Id: rs775690240
gnomAD v2: 19-7592467-C-G
gnomAD v3: 19-7527581-C-G
gnomAD v4: 19-7527581-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527581C>G , CM000681.2:g.7527581C>G GRCh38
NC_000019.9:g.7592467C>G , CM000681.1:g.7592467C>G GRCh37
NC_000019.8:g.7498467C>G NCBI36
NG_015806.1:g.9972C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.633C>G MANE Select ENSP00000264079.5:p.Leu211=
ENST00000264079.10:c.633C>G ENSP00000264079.5:p.Leu211=
ENST00000394321.9:n.713C>G
ENST00000598406.1:n.454C>G
ENST00000601003.1:c.572-283C>G ENSP00000469074.1:n.572-283C>G
NM_020533.2:c.633C>G NP_065394.1:p.Leu211=
NM_020533.3:c.633C>G MANE Select NP_065394.1:p.Leu211=