Canonical Allele Identifier: CA2320962438
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527690C= , CM000681.2:g.7527690C= GRCh38
NC_000019.9:g.7592576C= , CM000681.1:g.7592576C= GRCh37
NC_000019.8:g.7498576C= NCBI36
NG_015806.1:g.10081C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.680+62C= MANE Select ENSP00000264079.5:n.680+62C=
ENST00000264079.10:c.680+62C= ENSP00000264079.5:n.680+62C=
ENST00000394321.9:n.822C=
ENST00000598406.1:n.563C=
ENST00000601003.1:c.572-174C= ENSP00000469074.1:n.572-174C=
NM_020533.2:c.680+62C= NP_065394.1:n.680+62C=
NM_020533.3:c.680+62C= MANE Select NP_065394.1:n.680+62C=