Canonical Allele Identifier: CA403080661
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526446T>A , CM000681.2:g.7526446T>A GRCh38
NC_000019.9:g.7591332T>A , CM000681.1:g.7591332T>A GRCh37
NC_000019.8:g.7497332T>A NCBI36
NG_015806.1:g.8837T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.245T>A MANE Select ENSP00000264079.5:p.Leu82Gln
ENST00000264079.10:c.245T>A ENSP00000264079.5:p.Leu82Gln
ENST00000394321.9:n.325T>A
ENST00000596008.1:n.207T>A
ENST00000598406.1:n.66T>A
ENST00000601003.1:c.245T>A ENSP00000469074.1:p.Leu82Gln
NM_020533.2:c.245T>A NP_065394.1:p.Leu82Gln
NM_020533.3:c.245T>A MANE Select NP_065394.1:p.Leu82Gln