Canonical Allele Identifier: CA2320962611
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528006G= , CM000681.2:g.7528006G= GRCh38
NC_000019.9:g.7592892G= , CM000681.1:g.7592892G= GRCh37
NC_000019.8:g.7498892G= NCBI36
NG_015806.1:g.10397G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.777+46G= MANE Select ENSP00000264079.5:n.777+46G=
ENST00000264079.10:c.777+46G= ENSP00000264079.5:n.777+46G=
ENST00000394321.9:n.1092+46G=
NM_020533.2:c.777+46G= NP_065394.1:n.777+46G=
NM_020533.3:c.777+46G= MANE Select NP_065394.1:n.777+46G=