Canonical Allele Identifier: CA304894705
Gene: MCOLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2890884
ClinVar RCV Id: RCV003615182
dbSNP Id: rs999063846
gnomAD v3: 19-7525181-G-A
gnomAD v4: 19-7525181-G-A
MyVariant Identifiers: chr19:g.7590067G>A (hg19) chr19:g.7525181G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525181G>A , CM000681.2:g.7525181G>A GRCh38
NC_000019.9:g.7590067G>A , CM000681.1:g.7590067G>A GRCh37
NC_000019.8:g.7496067G>A NCBI36
NG_015806.1:g.7572G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.237+15G>A MANE Select ENSP00000264079.5:n.237+15G>A
ENST00000264079.10:c.237+15G>A ENSP00000264079.5:n.237+15G>A
ENST00000394321.9:n.317+15G>A
ENST00000596390.1:n.368G>A
ENST00000601003.1:c.237+15G>A ENSP00000469074.1:n.237+15G>A
NM_020533.2:c.237+15G>A NP_065394.1:n.237+15G>A
NM_020533.3:c.237+15G>A MANE Select NP_065394.1:n.237+15G>A
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