Canonical Allele Identifier: CA9138716
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs772567008
ExAC: 19:7591529 G / A
gnomAD v2: 19-7591529-G-A
gnomAD v4: 19-7526643-G-A
MyVariant Identifiers: chr19:g.7591529G>A (hg19) chr19:g.7526643G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526643G>A , CM000681.2:g.7526643G>A GRCh38
NC_000019.9:g.7591529G>A , CM000681.1:g.7591529G>A GRCh37
NC_000019.8:g.7497529G>A NCBI36
NG_015806.1:g.9034G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.405+37G>A MANE Select ENSP00000264079.5:n.405+37G>A
ENST00000264079.10:c.405+37G>A ENSP00000264079.5:n.405+37G>A
ENST00000394321.9:n.485+37G>A
ENST00000596008.1:n.367+37G>A
ENST00000598406.1:n.226+37G>A
ENST00000601003.1:c.405+37G>A ENSP00000469074.1:n.405+37G>A
NM_020533.2:c.405+37G>A NP_065394.1:n.405+37G>A
NM_020533.3:c.405+37G>A MANE Select NP_065394.1:n.405+37G>A
Search 100 bp 5'
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