Canonical Allele Identifier: CA2320963807
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530382C= , CM000681.2:g.7530382C= GRCh38
NC_000019.9:g.7595268C= , CM000681.1:g.7595268C= GRCh37
NC_000019.8:g.7501268C= NCBI36
NG_013374.1:g.1231C=
NG_015806.1:g.12773C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1456C= MANE Select ENSP00000264079.5:p.Arg486=
ENST00000264079.10:c.1456C= ENSP00000264079.5:p.Arg486=
ENST00000394321.9:n.1771C=
ENST00000594692.1:n.452C=
ENST00000595860.5:n.639C=
ENST00000599334.1:c.237-53C=
NM_020533.2:c.1456C= NP_065394.1:p.Arg486=
NM_020533.3:c.1456C= MANE Select NP_065394.1:p.Arg486=