Canonical Allele Identifier: CA9139262
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs770347734
gnomAD v2: 19-7598715-G-A
gnomAD v3: 19-7533829-G-A
gnomAD v4: 19-7533829-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533829G>A , CM000681.2:g.7533829G>A GRCh38
NC_000019.9:g.7598715G>A , CM000681.1:g.7598715G>A GRCh37
NC_000019.8:g.7504715G>A NCBI36
NG_013374.1:g.4678G>A
NG_015806.1:g.16220G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*34G>A MANE Select ENSP00000264079.5:n.*34G>A
ENST00000264079.10:c.*34G>A ENSP00000264079.5:n.*34G>A
ENST00000394321.9:n.2092G>A
ENST00000599334.1:c.505G>A
ENST00000601870.1:c.130G>A
ENST00000602227.1:n.331G>A
NM_020533.2:c.*34G>A NP_065394.1:n.*34G>A
NM_020533.3:c.*34G>A MANE Select NP_065394.1:n.*34G>A