Canonical Allele Identifier: CA2320965603
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533864T= , CM000681.2:g.7533864T= GRCh38
NC_000019.9:g.7598750T= , CM000681.1:g.7598750T= GRCh37
NC_000019.8:g.7504750T= NCBI36
NG_013374.1:g.4713T=
NG_015806.1:g.16255T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*69T= MANE Select ENSP00000264079.5:n.*69T=
ENST00000264079.10:c.*69T= ENSP00000264079.5:n.*69T=
ENST00000394321.9:n.2127T=
ENST00000599334.1:c.540T=
ENST00000601870.1:c.165T=
ENST00000602227.1:n.366T=
NM_020533.2:c.*69T= NP_065394.1:n.*69T=
NM_020533.3:c.*69T= MANE Select NP_065394.1:n.*69T=