Canonical Allele Identifier: CA2739637986
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527842C>A , CM000681.2:g.7527842C>A GRCh38
NC_000019.9:g.7592728C>A , CM000681.1:g.7592728C>A GRCh37
NC_000019.8:g.7498728C>A NCBI36
NG_015806.1:g.10233C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-22C>A MANE Select ENSP00000264079.5:n.681-22C>A
ENST00000264079.10:c.681-22C>A ENSP00000264079.5:n.681-22C>A
ENST00000394321.9:n.974C>A
ENST00000601003.1:c.572-22C>A ENSP00000469074.1:n.572-22C>A
NM_020533.2:c.681-22C>A NP_065394.1:n.681-22C>A
NM_020533.3:c.681-22C>A MANE Select NP_065394.1:n.681-22C>A
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