Canonical Allele Identifier: CA2320965568
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533823G= , CM000681.2:g.7533823G= GRCh38
NC_000019.9:g.7598709G= , CM000681.1:g.7598709G= GRCh37
NC_000019.8:g.7504709G= NCBI36
NG_013374.1:g.4672G=
NG_015806.1:g.16214G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*28G= MANE Select ENSP00000264079.5:n.*28G=
ENST00000264079.10:c.*28G= ENSP00000264079.5:n.*28G=
ENST00000394321.9:n.2086G=
ENST00000599334.1:c.499G=
ENST00000601870.1:c.124G=
ENST00000602227.1:n.325G=
NM_020533.2:c.*28G= NP_065394.1:n.*28G=
NM_020533.3:c.*28G= MANE Select NP_065394.1:n.*28G=