Canonical Allele Identifier: CA9138927
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs764072824
gnomAD v2: 19-7593128-A-G
gnomAD v3: 19-7528242-A-G
gnomAD v4: 19-7528242-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528242A>G , CM000681.2:g.7528242A>G GRCh38
NC_000019.9:g.7593128A>G , CM000681.1:g.7593128A>G GRCh37
NC_000019.8:g.7499128A>G NCBI36
NG_015806.1:g.10633A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.862A>G MANE Select ENSP00000264079.5:p.Ser288Gly
ENST00000264079.10:c.862A>G ENSP00000264079.5:p.Ser288Gly
ENST00000394321.9:n.1177A>G
NM_020533.2:c.862A>G NP_065394.1:p.Ser288Gly
NM_020533.3:c.862A>G MANE Select NP_065394.1:p.Ser288Gly