Canonical Allele Identifier: CA2320962532
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527844C= , CM000681.2:g.7527844C= GRCh38
NC_000019.9:g.7592730C= , CM000681.1:g.7592730C= GRCh37
NC_000019.8:g.7498730C= NCBI36
NG_015806.1:g.10235C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-20C= MANE Select ENSP00000264079.5:n.681-20C=
ENST00000264079.10:c.681-20C= ENSP00000264079.5:n.681-20C=
ENST00000394321.9:n.976C=
ENST00000601003.1:c.572-20C= ENSP00000469074.1:n.572-20C=
NM_020533.2:c.681-20C= NP_065394.1:n.681-20C=
NM_020533.3:c.681-20C= MANE Select NP_065394.1:n.681-20C=
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