Canonical Allele Identifier: CA2320965006
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022684787

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533086del , CM000681.2:g.7533086del GRCh38
NC_000019.9:g.7597972del , CM000681.1:g.7597972del GRCh37
NC_000019.8:g.7503972del NCBI36
NG_013374.1:g.3935del
NG_015806.1:g.15477del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1576-437del MANE Select ENSP00000264079.5:n.1576-437del
ENST00000264079.10:c.1576-437del ENSP00000264079.5:n.1576-437del
ENST00000394321.9:n.1891-437del
ENST00000599334.1:c.304-437del
NM_020533.2:c.1576-437del NP_065394.1:n.1576-437del
NM_020533.3:c.1576-437del MANE Select NP_065394.1:n.1576-437del