Canonical Allele Identifier: CA2576596902
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526339C>A , CM000681.2:g.7526339C>A GRCh38
NC_000019.9:g.7591225C>A , CM000681.1:g.7591225C>A GRCh37
NC_000019.8:g.7497225C>A NCBI36
NG_015806.1:g.8730C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.238-100C>A MANE Select ENSP00000264079.5:n.238-100C>A
ENST00000264079.10:c.238-100C>A ENSP00000264079.5:n.238-100C>A
ENST00000394321.9:n.318-100C>A
ENST00000596008.1:n.100C>A
ENST00000601003.1:c.238-100C>A ENSP00000469074.1:n.238-100C>A
NM_020533.2:c.238-100C>A NP_065394.1:n.238-100C>A
NM_020533.3:c.238-100C>A MANE Select NP_065394.1:n.238-100C>A
Search 100 bp 5'
Search 100 bp 3'