Canonical Allele Identifier: CA2320965142
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533384A= , CM000681.2:g.7533384A= GRCh38
NC_000019.9:g.7598270A= , CM000681.1:g.7598270A= GRCh37
NC_000019.8:g.7504270A= NCBI36
NG_013374.1:g.4233A=
NG_015806.1:g.15775A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1576-139A= MANE Select ENSP00000264079.5:n.1576-139A=
ENST00000264079.10:c.1576-139A= ENSP00000264079.5:n.1576-139A=
ENST00000394321.9:n.1891-139A=
ENST00000599334.1:c.304-139A=
NM_020533.2:c.1576-139A= NP_065394.1:n.1576-139A=
NM_020533.3:c.1576-139A= MANE Select NP_065394.1:n.1576-139A=