Canonical Allele Identifier: CA2576597018
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528004A>C , CM000681.2:g.7528004A>C GRCh38
NC_000019.9:g.7592890A>C , CM000681.1:g.7592890A>C GRCh37
NC_000019.8:g.7498890A>C NCBI36
NG_015806.1:g.10395A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.777+44A>C MANE Select ENSP00000264079.5:n.777+44A>C
ENST00000264079.10:c.777+44A>C ENSP00000264079.5:n.777+44A>C
ENST00000394321.9:n.1092+44A>C
NM_020533.2:c.777+44A>C NP_065394.1:n.777+44A>C
NM_020533.3:c.777+44A>C MANE Select NP_065394.1:n.777+44A>C