Canonical Allele Identifier: CA2320963141
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529116G= , CM000681.2:g.7529116G= GRCh38
NC_000019.9:g.7594002G= , CM000681.1:g.7594002G= GRCh37
NC_000019.8:g.7500002G= NCBI36
NG_015806.1:g.11507G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1150G= MANE Select ENSP00000264079.5:p.Asp384=
ENST00000264079.10:c.1150G= ENSP00000264079.5:p.Asp384=
ENST00000394321.9:n.1465G=
ENST00000594692.1:n.146G=
ENST00000595860.5:n.333G=
ENST00000599334.1:c.27G=
NM_020533.2:c.1150G= NP_065394.1:p.Asp384=
NM_020533.3:c.1150G= MANE Select NP_065394.1:p.Asp384=