Canonical Allele Identifier: CA304853491
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs923499382
gnomAD v2: 19-7592576-C-T
gnomAD v3: 19-7527690-C-T
gnomAD v4: 19-7527690-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527690C>T , CM000681.2:g.7527690C>T GRCh38
NC_000019.9:g.7592576C>T , CM000681.1:g.7592576C>T GRCh37
NC_000019.8:g.7498576C>T NCBI36
NG_015806.1:g.10081C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.680+62C>T MANE Select ENSP00000264079.5:n.680+62C>T
ENST00000264079.10:c.680+62C>T ENSP00000264079.5:n.680+62C>T
ENST00000394321.9:n.822C>T
ENST00000598406.1:n.563C>T
ENST00000601003.1:c.572-174C>T ENSP00000469074.1:n.572-174C>T
NM_020533.2:c.680+62C>T NP_065394.1:n.680+62C>T
NM_020533.3:c.680+62C>T MANE Select NP_065394.1:n.680+62C>T