Canonical Allele Identifier: CA403087138
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7594089G>A (hg19) chr19:g.7529203G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529203G>A , CM000681.2:g.7529203G>A GRCh38
NC_000019.9:g.7594089G>A , CM000681.1:g.7594089G>A GRCh37
NC_000019.8:g.7500089G>A NCBI36
NG_013374.1:g.52G>A
NG_015806.1:g.11594G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1236+1G>A MANE Select ENSP00000264079.5:n.1236+1G>A
ENST00000264079.10:c.1236+1G>A ENSP00000264079.5:n.1236+1G>A
ENST00000394321.9:n.1551+1G>A
ENST00000594692.1:n.232+1G>A
ENST00000595860.5:n.419+1G>A
ENST00000599334.1:c.113+1G>A
NM_020533.2:c.1236+1G>A NP_065394.1:n.1236+1G>A
NM_020533.3:c.1236+1G>A MANE Select NP_065394.1:n.1236+1G>A
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