Canonical Allele Identifier: CA2320961941
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526719G= , CM000681.2:g.7526719G= GRCh38
NC_000019.9:g.7591605G= , CM000681.1:g.7591605G= GRCh37
NC_000019.8:g.7497605G= NCBI36
NG_015806.1:g.9110G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.406-42G= MANE Select ENSP00000264079.5:n.406-42G=
ENST00000264079.10:c.406-42G= ENSP00000264079.5:n.406-42G=
ENST00000394321.9:n.486-42G=
ENST00000596008.1:n.368-42G=
ENST00000598406.1:n.227-42G=
ENST00000601003.1:c.406-42G= ENSP00000469074.1:n.406-42G=
NM_020533.2:c.406-42G= NP_065394.1:n.406-42G=
NM_020533.3:c.406-42G= MANE Select NP_065394.1:n.406-42G=
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