Canonical Allele Identifier: CA2521503455
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528443G>T , CM000681.2:g.7528443G>T GRCh38
NC_000019.9:g.7593329G>T , CM000681.1:g.7593329G>T GRCh37
NC_000019.8:g.7499329G>T NCBI36
NG_015806.1:g.10834G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.878-154G>T MANE Select ENSP00000264079.5:n.878-154G>T
ENST00000264079.10:c.878-154G>T ENSP00000264079.5:n.878-154G>T
ENST00000394321.9:n.1193-154G>T
NM_020533.2:c.878-154G>T NP_065394.1:n.878-154G>T
NM_020533.3:c.878-154G>T MANE Select NP_065394.1:n.878-154G>T