Canonical Allele Identifier: CA403081426
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022578631
gnomAD v3: 19-7526837-C-G
gnomAD v4: 19-7526837-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526837C>G , CM000681.2:g.7526837C>G GRCh38
NC_000019.9:g.7591723C>G , CM000681.1:g.7591723C>G GRCh37
NC_000019.8:g.7497723C>G NCBI36
NG_015806.1:g.9228C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.482C>G MANE Select ENSP00000264079.5:p.Ser161Ter
ENST00000264079.10:c.482C>G ENSP00000264079.5:p.Ser161Ter
ENST00000394321.9:n.562C>G
ENST00000596008.1:n.444C>G
ENST00000598406.1:n.303C>G
ENST00000601003.1:c.482C>G ENSP00000469074.1:p.Ser161Ter
NM_020533.2:c.482C>G NP_065394.1:p.Ser161Ter
NM_020533.3:c.482C>G MANE Select NP_065394.1:p.Ser161Ter