Canonical Allele Identifier: CA9138591
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs759555730
gnomAD v2: 19-7589874-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7524988C>G , CM000681.2:g.7524988C>G GRCh38
NC_000019.9:g.7589874C>G , CM000681.1:g.7589874C>G GRCh37
NC_000019.8:g.7495874C>G NCBI36
NG_015806.1:g.7379C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.59C>G MANE Select ENSP00000264079.5:p.Pro20Arg
ENST00000264079.10:c.59C>G ENSP00000264079.5:p.Pro20Arg
ENST00000394321.9:n.139C>G
ENST00000596390.1:n.175C>G
ENST00000601003.1:c.59C>G ENSP00000469074.1:p.Pro20Arg
NM_020533.2:c.59C>G NP_065394.1:p.Pro20Arg
NM_020533.3:c.59C>G MANE Select NP_065394.1:p.Pro20Arg