Canonical Allele Identifier: CA2320963140
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529115C= , CM000681.2:g.7529115C= GRCh38
NC_000019.9:g.7594001C= , CM000681.1:g.7594001C= GRCh37
NC_000019.8:g.7500001C= NCBI36
NG_015806.1:g.11506C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1149C= MANE Select ENSP00000264079.5:p.Tyr383=
ENST00000264079.10:c.1149C= ENSP00000264079.5:p.Tyr383=
ENST00000394321.9:n.1464C=
ENST00000594692.1:n.145C=
ENST00000595860.5:n.332C=
ENST00000599334.1:c.26C=
NM_020533.2:c.1149C= NP_065394.1:p.Tyr383=
NM_020533.3:c.1149C= MANE Select NP_065394.1:p.Tyr383=