Canonical Allele Identifier: CA9138872
Gene: MCOLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1568828
ClinVar RCV Id: RCV002218641
dbSNP Id: rs371978455
ExAC: 19:7592735 G / A
gnomAD v2: 19-7592735-G-A
gnomAD v3: 19-7527849-G-A
gnomAD v4: 19-7527849-G-A
MyVariant Identifiers: chr19:g.7592735G>A (hg19) chr19:g.7527849G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527849G>A , CM000681.2:g.7527849G>A GRCh38
NC_000019.9:g.7592735G>A , CM000681.1:g.7592735G>A GRCh37
NC_000019.8:g.7498735G>A NCBI36
NG_015806.1:g.10240G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-15G>A MANE Select ENSP00000264079.5:n.681-15G>A
ENST00000264079.10:c.681-15G>A ENSP00000264079.5:n.681-15G>A
ENST00000394321.9:n.981G>A
ENST00000601003.1:c.572-15G>A ENSP00000469074.1:n.572-15G>A
NM_020533.2:c.681-15G>A NP_065394.1:n.681-15G>A
NM_020533.3:c.681-15G>A MANE Select NP_065394.1:n.681-15G>A
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