Canonical Allele Identifier: CA2320965563
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533815G= , CM000681.2:g.7533815G= GRCh38
NC_000019.9:g.7598701G= , CM000681.1:g.7598701G= GRCh37
NC_000019.8:g.7504701G= NCBI36
NG_013374.1:g.4664G=
NG_015806.1:g.16206G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*20G= MANE Select ENSP00000264079.5:n.*20G=
ENST00000264079.10:c.*20G= ENSP00000264079.5:n.*20G=
ENST00000394321.9:n.2078G=
ENST00000599334.1:c.491G=
ENST00000601870.1:c.116G=
ENST00000602227.1:n.317G=
NM_020533.2:c.*20G= NP_065394.1:n.*20G=
NM_020533.3:c.*20G= MANE Select NP_065394.1:n.*20G=