Canonical Allele Identifier: CA505403434
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1400844011
gnomAD v2: 19-7593871-C-T
gnomAD v4: 19-7528985-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528985C>T , CM000681.2:g.7528985C>T GRCh38
NC_000019.9:g.7593871C>T , CM000681.1:g.7593871C>T GRCh37
NC_000019.8:g.7499871C>T NCBI36
NG_015806.1:g.11376C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1134+15C>T MANE Select ENSP00000264079.5:n.1134+15C>T
ENST00000264079.10:c.1134+15C>T ENSP00000264079.5:n.1134+15C>T
ENST00000394321.9:n.1449+15C>T
ENST00000594692.1:n.15C>T
ENST00000595860.5:n.317+15C>T
ENST00000599334.1:c.11+15C>T
NM_020533.2:c.1134+15C>T NP_065394.1:n.1134+15C>T
NM_020533.3:c.1134+15C>T MANE Select NP_065394.1:n.1134+15C>T