Canonical Allele Identifier: CA2320963814
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530391C= , CM000681.2:g.7530391C= GRCh38
NC_000019.9:g.7595277C= , CM000681.1:g.7595277C= GRCh37
NC_000019.8:g.7501277C= NCBI36
NG_013374.1:g.1240C=
NG_015806.1:g.12782C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1465C= MANE Select ENSP00000264079.5:p.Leu489=
ENST00000264079.10:c.1465C= ENSP00000264079.5:p.Leu489=
ENST00000394321.9:n.1780C=
ENST00000594692.1:n.461C=
ENST00000595860.5:n.648C=
ENST00000599334.1:c.237-44C=
NM_020533.2:c.1465C= NP_065394.1:p.Leu489=
NM_020533.3:c.1465C= MANE Select NP_065394.1:p.Leu489=