Canonical Allele Identifier: CA631318863
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1321143364
gnomAD v2: 19-7595112-C-A
gnomAD v3: 19-7530226-C-A
gnomAD v4: 19-7530226-C-A
MyVariant Identifiers: chr19:g.7595112C>A (hg19) chr19:g.7530226C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530226C>A , CM000681.2:g.7530226C>A GRCh38
NC_000019.9:g.7595112C>A , CM000681.1:g.7595112C>A GRCh37
NC_000019.8:g.7501112C>A NCBI36
NG_013374.1:g.1075C>A
NG_015806.1:g.12617C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-60C>A MANE Select ENSP00000264079.5:n.1360-60C>A
ENST00000264079.10:c.1360-60C>A ENSP00000264079.5:n.1360-60C>A
ENST00000394321.9:n.1675-60C>A
ENST00000594692.1:n.356-60C>A
ENST00000595860.5:n.543-60C>A
ENST00000599334.1:c.237-209C>A
NM_020533.2:c.1360-60C>A NP_065394.1:n.1360-60C>A
NM_020533.3:c.1360-60C>A MANE Select NP_065394.1:n.1360-60C>A
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