Canonical Allele Identifier: CA2320963525
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529871A= , CM000681.2:g.7529871A= GRCh38
NC_000019.9:g.7594757A= , CM000681.1:g.7594757A= GRCh37
NC_000019.8:g.7500757A= NCBI36
NG_013374.1:g.720A=
NG_015806.1:g.12262A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1359+159A= MANE Select ENSP00000264079.5:n.1359+159A=
ENST00000264079.10:c.1359+159A= ENSP00000264079.5:n.1359+159A=
ENST00000394321.9:n.1674+159A=
ENST00000594692.1:n.355+159A=
ENST00000595860.5:n.542+159A=
ENST00000599334.1:c.236+159A=
NM_020533.2:c.1359+159A= NP_065394.1:n.1359+159A=
NM_020533.3:c.1359+159A= MANE Select NP_065394.1:n.1359+159A=