Canonical Allele Identifier: CA2320963805
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530380G= , CM000681.2:g.7530380G= GRCh38
NC_000019.9:g.7595266G= , CM000681.1:g.7595266G= GRCh37
NC_000019.8:g.7501266G= NCBI36
NG_013374.1:g.1229G=
NG_015806.1:g.12771G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1454G= MANE Select ENSP00000264079.5:p.Gly485=
ENST00000264079.10:c.1454G= ENSP00000264079.5:p.Gly485=
ENST00000394321.9:n.1769G=
ENST00000594692.1:n.450G=
ENST00000595860.5:n.637G=
ENST00000599334.1:c.237-55G=
NM_020533.2:c.1454G= NP_065394.1:p.Gly485=
NM_020533.3:c.1454G= MANE Select NP_065394.1:p.Gly485=