Canonical Allele Identifier: CA2320962528
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022594803

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527837del , CM000681.2:g.7527837del GRCh38
NC_000019.9:g.7592723del , CM000681.1:g.7592723del GRCh37
NC_000019.8:g.7498723del NCBI36
NG_015806.1:g.10228del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-27del MANE Select ENSP00000264079.5:n.681-27del
ENST00000264079.10:c.681-27del ENSP00000264079.5:n.681-27del
ENST00000394321.9:n.969del
ENST00000601003.1:c.572-27del ENSP00000469074.1:n.572-27del
NM_020533.2:c.681-27del NP_065394.1:n.681-27del
NM_020533.3:c.681-27del MANE Select NP_065394.1:n.681-27del