Canonical Allele Identifier: CA2587950399
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7533856-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533856C>T , CM000681.2:g.7533856C>T GRCh38
NC_000019.9:g.7598742C>T , CM000681.1:g.7598742C>T GRCh37
NC_000019.8:g.7504742C>T NCBI36
NG_013374.1:g.4705C>T
NG_015806.1:g.16247C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*61C>T MANE Select ENSP00000264079.5:n.*61C>T
ENST00000264079.10:c.*61C>T ENSP00000264079.5:n.*61C>T
ENST00000394321.9:n.2119C>T
ENST00000599334.1:c.532C>T
ENST00000601870.1:c.157C>T
ENST00000602227.1:n.358C>T
NM_020533.2:c.*61C>T NP_065394.1:n.*61C>T
NM_020533.3:c.*61C>T MANE Select NP_065394.1:n.*61C>T
Search 100 bp 5'
Search 100 bp 3'