Canonical Allele Identifier: CA2320965567
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533819G= , CM000681.2:g.7533819G= GRCh38
NC_000019.9:g.7598705G= , CM000681.1:g.7598705G= GRCh37
NC_000019.8:g.7504705G= NCBI36
NG_013374.1:g.4668G=
NG_015806.1:g.16210G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*24G= MANE Select ENSP00000264079.5:n.*24G=
ENST00000264079.10:c.*24G= ENSP00000264079.5:n.*24G=
ENST00000394321.9:n.2082G=
ENST00000599334.1:c.495G=
ENST00000601870.1:c.120G=
ENST00000602227.1:n.321G=
NM_020533.2:c.*24G= NP_065394.1:n.*24G=
NM_020533.3:c.*24G= MANE Select NP_065394.1:n.*24G=