Canonical Allele Identifier: CA631317852
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1408307310
gnomAD v2: 19-7592330-G-A
gnomAD v3: 19-7527444-G-A
gnomAD v4: 19-7527444-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527444G>A , CM000681.2:g.7527444G>A GRCh38
NC_000019.9:g.7592330G>A , CM000681.1:g.7592330G>A GRCh37
NC_000019.8:g.7498330G>A NCBI36
NG_015806.1:g.9835G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.572-76G>A MANE Select ENSP00000264079.5:n.572-76G>A
ENST00000264079.10:c.572-76G>A ENSP00000264079.5:n.572-76G>A
ENST00000394321.9:n.652-76G>A
ENST00000598406.1:n.393-76G>A
ENST00000601003.1:c.572-420G>A ENSP00000469074.1:n.572-420G>A
NM_020533.2:c.572-76G>A NP_065394.1:n.572-76G>A
NM_020533.3:c.572-76G>A MANE Select NP_065394.1:n.572-76G>A