Canonical Allele Identifier: CA2580097123
Gene: MCOLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1940400
ClinVar RCV Id: RCV002658378
gnomAD v4: 19-7528711-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528711T>G , CM000681.2:g.7528711T>G GRCh38
NC_000019.9:g.7593597T>G , CM000681.1:g.7593597T>G GRCh37
NC_000019.8:g.7499597T>G NCBI36
NG_015806.1:g.11102T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.984+8T>G MANE Select ENSP00000264079.5:n.984+8T>G
ENST00000264079.10:c.984+8T>G ENSP00000264079.5:n.984+8T>G
ENST00000394321.9:n.1299+8T>G
ENST00000595860.5:n.58T>G
NM_020533.2:c.984+8T>G NP_065394.1:n.984+8T>G
NM_020533.3:c.984+8T>G MANE Select NP_065394.1:n.984+8T>G
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