Canonical Allele Identifier: CA2320962709
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.862A= MANE Select ENSP00000264079.5:p.Ser288=
ENST00000264079.10:c.862A= ENSP00000264079.5:p.Ser288=
ENST00000394321.9:n.1177A=
NM_020533.2:c.862A= NP_065394.1:p.Ser288=
NM_020533.3:c.862A= MANE Select NP_065394.1:p.Ser288=