Canonical Allele Identifier: CA2320962002
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526854C= , CM000681.2:g.7526854C= GRCh38
NC_000019.9:g.7591740C= , CM000681.1:g.7591740C= GRCh37
NC_000019.8:g.7497740C= NCBI36
NG_015806.1:g.9245C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.499C= MANE Select ENSP00000264079.5:p.Gln167=
ENST00000264079.10:c.499C= ENSP00000264079.5:p.Gln167=
ENST00000394321.9:n.579C=
ENST00000596008.1:n.461C=
ENST00000598406.1:n.320C=
ENST00000601003.1:c.499C= ENSP00000469074.1:p.Gln167=
NM_020533.2:c.499C= NP_065394.1:p.Gln167=
NM_020533.3:c.499C= MANE Select NP_065394.1:p.Gln167=