Canonical Allele Identifier: CA2320961783
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526440T= , CM000681.2:g.7526440T= GRCh38
NC_000019.9:g.7591326T= , CM000681.1:g.7591326T= GRCh37
NC_000019.8:g.7497326T= NCBI36
NG_015806.1:g.8831T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.239T= MANE Select ENSP00000264079.5:p.Leu80=
ENST00000264079.10:c.239T= ENSP00000264079.5:p.Leu80=
ENST00000394321.9:n.319T=
ENST00000596008.1:n.201T=
ENST00000598406.1:n.60T=
ENST00000601003.1:c.239T= ENSP00000469074.1:p.Leu80=
NM_020533.2:c.239T= NP_065394.1:p.Leu80=
NM_020533.3:c.239T= MANE Select NP_065394.1:p.Leu80=