Canonical Allele Identifier: CA9139058
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs757251025
gnomAD v2: 19-7593963-G-A
gnomAD v3: 19-7529077-G-A
gnomAD v4: 19-7529077-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529077G>A , CM000681.2:g.7529077G>A GRCh38
NC_000019.9:g.7593963G>A , CM000681.1:g.7593963G>A GRCh37
NC_000019.8:g.7499963G>A NCBI36
NG_015806.1:g.11468G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1135-24G>A MANE Select ENSP00000264079.5:n.1135-24G>A
ENST00000264079.10:c.1135-24G>A ENSP00000264079.5:n.1135-24G>A
ENST00000394321.9:n.1450-24G>A
ENST00000594692.1:n.107G>A
ENST00000595860.5:n.318-24G>A
ENST00000599334.1:c.12-24G>A
NM_020533.2:c.1135-24G>A NP_065394.1:n.1135-24G>A
NM_020533.3:c.1135-24G>A MANE Select NP_065394.1:n.1135-24G>A