Canonical Allele Identifier: CA2587947876
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7526654-CGGGCAGGTGCAGTTGGGCGGGCAGGTGCTGGTGGGCGGGCAGGTGCAGGTGGGT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526659_7526712del , CM000681.2:g.7526659_7526712del GRCh38
NC_000019.9:g.7591545_7591598del , CM000681.1:g.7591545_7591598del GRCh37
NC_000019.8:g.7497545_7497598del NCBI36
NG_015806.1:g.9050_9103del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.405+53_406-49del MANE Select ENSP00000264079.5:n.405+53_406-49del
ENST00000264079.10:c.405+53_406-49del ENSP00000264079.5:n.405+53_406-49del
ENST00000394321.9:n.485+53_486-49del
ENST00000596008.1:n.367+53_368-49del
ENST00000598406.1:n.226+53_227-49del
ENST00000601003.1:c.405+53_406-49del ENSP00000469074.1:n.405+53_406-49del
NM_020533.2:c.405+53_406-49del NP_065394.1:n.405+53_406-49del
NM_020533.3:c.405+53_406-49del MANE Select NP_065394.1:n.405+53_406-49del
Search 100 bp 5'
Search 100 bp 3'