Canonical Allele Identifier: CA2320965590
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533851G= , CM000681.2:g.7533851G= GRCh38
NC_000019.9:g.7598737G= , CM000681.1:g.7598737G= GRCh37
NC_000019.8:g.7504737G= NCBI36
NG_013374.1:g.4700G=
NG_015806.1:g.16242G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*56G= MANE Select ENSP00000264079.5:n.*56G=
ENST00000264079.10:c.*56G= ENSP00000264079.5:n.*56G=
ENST00000394321.9:n.2114G=
ENST00000599334.1:c.527G=
ENST00000601870.1:c.152G=
ENST00000602227.1:n.353G=
NM_020533.2:c.*56G= NP_065394.1:n.*56G=
NM_020533.3:c.*56G= MANE Select NP_065394.1:n.*56G=