Canonical Allele Identifier: CA2587950384
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7533821-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533821A>C , CM000681.2:g.7533821A>C GRCh38
NC_000019.9:g.7598707A>C , CM000681.1:g.7598707A>C GRCh37
NC_000019.8:g.7504707A>C NCBI36
NG_013374.1:g.4670A>C
NG_015806.1:g.16212A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*26A>C MANE Select ENSP00000264079.5:n.*26A>C
ENST00000264079.10:c.*26A>C ENSP00000264079.5:n.*26A>C
ENST00000394321.9:n.2084A>C
ENST00000599334.1:c.497A>C
ENST00000601870.1:c.122A>C
ENST00000602227.1:n.323A>C
NM_020533.2:c.*26A>C NP_065394.1:n.*26A>C
NM_020533.3:c.*26A>C MANE Select NP_065394.1:n.*26A>C
Search 100 bp 5'
Search 100 bp 3'