Canonical Allele Identifier: CA403084911
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs764072824
gnomAD v2: 19-7593128-A-T

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.862A>T MANE Select ENSP00000264079.5:p.Ser288Cys
ENST00000264079.10:c.862A>T ENSP00000264079.5:p.Ser288Cys
ENST00000394321.9:n.1177A>T
NM_020533.2:c.862A>T NP_065394.1:p.Ser288Cys
NM_020533.3:c.862A>T MANE Select NP_065394.1:p.Ser288Cys