Canonical Allele Identifier: CA9138607
Gene: MCOLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1417768
ClinVar RCV Id: RCV001951869
dbSNP Id: rs773313990
ExAC: 19:7589905 G / A
gnomAD v2: 19-7589905-G-A
gnomAD v3: 19-7525019-G-A
gnomAD v4: 19-7525019-G-A
MyVariant Identifiers: chr19:g.7589905G>A (hg19) chr19:g.7525019G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525019G>A , CM000681.2:g.7525019G>A GRCh38
NC_000019.9:g.7589905G>A , CM000681.1:g.7589905G>A GRCh37
NC_000019.8:g.7495905G>A NCBI36
NG_015806.1:g.7410G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.90G>A MANE Select ENSP00000264079.5:p.Pro30=
ENST00000264079.10:c.90G>A ENSP00000264079.5:p.Pro30=
ENST00000394321.9:n.170G>A
ENST00000596390.1:n.206G>A
ENST00000601003.1:c.90G>A ENSP00000469074.1:p.Pro30=
NM_020533.2:c.90G>A NP_065394.1:p.Pro30=
NM_020533.3:c.90G>A MANE Select NP_065394.1:p.Pro30=
Search 100 bp 5'
Search 100 bp 3'