Canonical Allele Identifier: CA403081527
Gene: MCOLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1460387
ClinVar RCV Id: RCV001963290
dbSNP Id: rs896210352

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526862C>G , CM000681.2:g.7526862C>G GRCh38
NC_000019.9:g.7591748C>G , CM000681.1:g.7591748C>G GRCh37
NC_000019.8:g.7497748C>G NCBI36
NG_015806.1:g.9253C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.507C>G MANE Select ENSP00000264079.5:p.Tyr169Ter
ENST00000264079.10:c.507C>G ENSP00000264079.5:p.Tyr169Ter
ENST00000394321.9:n.587C>G
ENST00000596008.1:n.469C>G
ENST00000598406.1:n.328C>G
ENST00000601003.1:c.507C>G ENSP00000469074.1:p.Tyr169Ter
NM_020533.2:c.507C>G NP_065394.1:p.Tyr169Ter
NM_020533.3:c.507C>G MANE Select NP_065394.1:p.Tyr169Ter