Canonical Allele Identifier: CA304854382
Gene: MCOLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 991188
ClinVar RCV Id: RCV001279359
dbSNP Id: rs201195245
gnomAD v4: 19-7528915-C-T
MyVariant Identifiers: chr19:g.7593801C>T (hg19) chr19:g.7528915C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528915C>T , CM000681.2:g.7528915C>T GRCh38
NC_000019.9:g.7593801C>T , CM000681.1:g.7593801C>T GRCh37
NC_000019.8:g.7499801C>T NCBI36
NG_015806.1:g.11306C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1079C>T MANE Select ENSP00000264079.5:p.Thr360Ile
ENST00000264079.10:c.1079C>T ENSP00000264079.5:p.Thr360Ile
ENST00000394321.9:n.1394C>T
ENST00000595860.5:n.262C>T
NM_020533.2:c.1079C>T NP_065394.1:p.Thr360Ile
NM_020533.3:c.1079C>T MANE Select NP_065394.1:p.Thr360Ile
Search 100 bp 5'
Search 100 bp 3'