Canonical Allele Identifier: CA403089592
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530373C>G , CM000681.2:g.7530373C>G GRCh38
NC_000019.9:g.7595259C>G , CM000681.1:g.7595259C>G GRCh37
NC_000019.8:g.7501259C>G NCBI36
NG_013374.1:g.1222C>G
NG_015806.1:g.12764C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1447C>G MANE Select ENSP00000264079.5:p.Gln483Glu
ENST00000264079.10:c.1447C>G ENSP00000264079.5:p.Gln483Glu
ENST00000394321.9:n.1762C>G
ENST00000594692.1:n.443C>G
ENST00000595860.5:n.630C>G
ENST00000599334.1:c.237-62C>G
NM_020533.2:c.1447C>G NP_065394.1:p.Gln483Glu
NM_020533.3:c.1447C>G MANE Select NP_065394.1:p.Gln483Glu