Canonical Allele Identifier: CA2320963170
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529180T= , CM000681.2:g.7529180T= GRCh38
NC_000019.9:g.7594066T= , CM000681.1:g.7594066T= GRCh37
NC_000019.8:g.7500066T= NCBI36
NG_013374.1:g.29T=
NG_015806.1:g.11571T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1214T= MANE Select ENSP00000264079.5:p.Leu405=
ENST00000264079.10:c.1214T= ENSP00000264079.5:p.Leu405=
ENST00000394321.9:n.1529T=
ENST00000594692.1:n.210T=
ENST00000595860.5:n.397T=
ENST00000599334.1:c.91T=
NM_020533.2:c.1214T= NP_065394.1:p.Leu405=
NM_020533.3:c.1214T= MANE Select NP_065394.1:p.Leu405=