Canonical Allele Identifier: CA2320965605
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533870T= , CM000681.2:g.7533870T= GRCh38
NC_000019.9:g.7598756T= , CM000681.1:g.7598756T= GRCh37
NC_000019.8:g.7504756T= NCBI36
NG_013374.1:g.4719T=
NG_015806.1:g.16261T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*75T= MANE Select ENSP00000264079.5:n.*75T=
ENST00000264079.10:c.*75T= ENSP00000264079.5:n.*75T=
ENST00000394321.9:n.2133T=
ENST00000599334.1:c.546T=
ENST00000601870.1:c.169+2T=
ENST00000602227.1:n.372T=
NM_020533.2:c.*75T= NP_065394.1:n.*75T=
NM_020533.3:c.*75T= MANE Select NP_065394.1:n.*75T=