Canonical Allele Identifier: CA2320962534
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527845A= , CM000681.2:g.7527845A= GRCh38
NC_000019.9:g.7592731A= , CM000681.1:g.7592731A= GRCh37
NC_000019.8:g.7498731A= NCBI36
NG_015806.1:g.10236A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-19A= MANE Select ENSP00000264079.5:n.681-19A=
ENST00000264079.10:c.681-19A= ENSP00000264079.5:n.681-19A=
ENST00000394321.9:n.977A=
ENST00000601003.1:c.572-19A= ENSP00000469074.1:n.572-19A=
NM_020533.2:c.681-19A= NP_065394.1:n.681-19A=
NM_020533.3:c.681-19A= MANE Select NP_065394.1:n.681-19A=
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