Canonical Allele Identifier: CA2320965023
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533136C= , CM000681.2:g.7533136C= GRCh38
NC_000019.9:g.7598022C= , CM000681.1:g.7598022C= GRCh37
NC_000019.8:g.7504022C= NCBI36
NG_013374.1:g.3985C=
NG_015806.1:g.15527C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1576-387C= MANE Select ENSP00000264079.5:n.1576-387C=
ENST00000264079.10:c.1576-387C= ENSP00000264079.5:n.1576-387C=
ENST00000394321.9:n.1891-387C=
ENST00000599334.1:c.304-387C=
NM_020533.2:c.1576-387C= NP_065394.1:n.1576-387C=
NM_020533.3:c.1576-387C= MANE Select NP_065394.1:n.1576-387C=