Canonical Allele Identifier: CA9138844
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs777513647
gnomAD v2: 19-7592617-G-A
gnomAD v3: 19-7527731-G-A
gnomAD v4: 19-7527731-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527731G>A , CM000681.2:g.7527731G>A GRCh38
NC_000019.9:g.7592617G>A , CM000681.1:g.7592617G>A GRCh37
NC_000019.8:g.7498617G>A NCBI36
NG_015806.1:g.10122G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.680+103G>A MANE Select ENSP00000264079.5:n.680+103G>A
ENST00000264079.10:c.680+103G>A ENSP00000264079.5:n.680+103G>A
ENST00000394321.9:n.863G>A
ENST00000598406.1:n.604G>A
ENST00000601003.1:c.572-133G>A ENSP00000469074.1:n.572-133G>A
NM_020533.2:c.680+103G>A NP_065394.1:n.680+103G>A
NM_020533.3:c.680+103G>A MANE Select NP_065394.1:n.680+103G>A