Canonical Allele Identifier: CA2320963772
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530290G= , CM000681.2:g.7530290G= GRCh38
NC_000019.9:g.7595176G= , CM000681.1:g.7595176G= GRCh37
NC_000019.8:g.7501176G= NCBI36
NG_013374.1:g.1139G=
NG_015806.1:g.12681G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1364G= MANE Select ENSP00000264079.5:p.Arg455=
ENST00000264079.10:c.1364G= ENSP00000264079.5:p.Arg455=
ENST00000394321.9:n.1679G=
ENST00000594692.1:n.360G=
ENST00000595860.5:n.547G=
ENST00000599334.1:c.237-145G=
NM_020533.2:c.1364G= NP_065394.1:p.Arg455=
NM_020533.3:c.1364G= MANE Select NP_065394.1:p.Arg455=