Canonical Allele Identifier: CA2841549196
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529044C>A , CM000681.2:g.7529044C>A GRCh38
NC_000019.9:g.7593930C>A , CM000681.1:g.7593930C>A GRCh37
NC_000019.8:g.7499930C>A NCBI36
NG_015806.1:g.11435C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1135-57C>A MANE Select ENSP00000264079.5:n.1135-57C>A
ENST00000264079.10:c.1135-57C>A ENSP00000264079.5:n.1135-57C>A
ENST00000394321.9:n.1450-57C>A
ENST00000594692.1:n.74C>A
ENST00000595860.5:n.318-57C>A
ENST00000599334.1:c.12-57C>A
NM_020533.2:c.1135-57C>A NP_065394.1:n.1135-57C>A
NM_020533.3:c.1135-57C>A MANE Select NP_065394.1:n.1135-57C>A