Canonical Allele Identifier: CA2320962198
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527241C= , CM000681.2:g.7527241C= GRCh38
NC_000019.9:g.7592127C= , CM000681.1:g.7592127C= GRCh37
NC_000019.8:g.7498127C= NCBI36
NG_015806.1:g.9632C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.572-279C= MANE Select ENSP00000264079.5:n.572-279C=
ENST00000264079.10:c.572-279C= ENSP00000264079.5:n.572-279C=
ENST00000394321.9:n.652-279C=
ENST00000598406.1:n.393-279C=
ENST00000601003.1:c.571+315C= ENSP00000469074.1:n.571+315C=
NM_020533.2:c.572-279C= NP_065394.1:n.572-279C=
NM_020533.3:c.572-279C= MANE Select NP_065394.1:n.572-279C=
Search 100 bp 5'
Search 100 bp 3'