Canonical Allele Identifier: CA2576597017
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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