Canonical Allele Identifier: CA2320961253
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525050C= , CM000681.2:g.7525050C= GRCh38
NC_000019.9:g.7589936C= , CM000681.1:g.7589936C= GRCh37
NC_000019.8:g.7495936C= NCBI36
NG_015806.1:g.7441C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.121C= MANE Select ENSP00000264079.5:p.Leu41=
ENST00000264079.10:c.121C= ENSP00000264079.5:p.Leu41=
ENST00000394321.9:n.201C=
ENST00000596390.1:n.237C=
ENST00000601003.1:c.121C= ENSP00000469074.1:p.Leu41=
NM_020533.2:c.121C= NP_065394.1:p.Leu41=
NM_020533.3:c.121C= MANE Select NP_065394.1:p.Leu41=