Canonical Allele Identifier: CA2739637886
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527767G>T , CM000681.2:g.7527767G>T GRCh38
NC_000019.9:g.7592653G>T , CM000681.1:g.7592653G>T GRCh37
NC_000019.8:g.7498653G>T NCBI36
NG_015806.1:g.10158G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-97G>T MANE Select ENSP00000264079.5:n.681-97G>T
ENST00000264079.10:c.681-97G>T ENSP00000264079.5:n.681-97G>T
ENST00000394321.9:n.899G>T
ENST00000598406.1:n.640G>T
ENST00000601003.1:c.572-97G>T ENSP00000469074.1:n.572-97G>T
NM_020533.2:c.681-97G>T NP_065394.1:n.681-97G>T
NM_020533.3:c.681-97G>T MANE Select NP_065394.1:n.681-97G>T