Canonical Allele Identifier: CA2320962446
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527696C= , CM000681.2:g.7527696C= GRCh38
NC_000019.9:g.7592582C= , CM000681.1:g.7592582C= GRCh37
NC_000019.8:g.7498582C= NCBI36
NG_015806.1:g.10087C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.680+68C= MANE Select ENSP00000264079.5:n.680+68C=
ENST00000264079.10:c.680+68C= ENSP00000264079.5:n.680+68C=
ENST00000394321.9:n.828C=
ENST00000598406.1:n.569C=
ENST00000601003.1:c.572-168C= ENSP00000469074.1:n.572-168C=
NM_020533.2:c.680+68C= NP_065394.1:n.680+68C=
NM_020533.3:c.680+68C= MANE Select NP_065394.1:n.680+68C=