Canonical Allele Identifier: CA2739637883
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527763C>G , CM000681.2:g.7527763C>G GRCh38
NC_000019.9:g.7592649C>G , CM000681.1:g.7592649C>G GRCh37
NC_000019.8:g.7498649C>G NCBI36
NG_015806.1:g.10154C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-101C>G MANE Select ENSP00000264079.5:n.681-101C>G
ENST00000264079.10:c.681-101C>G ENSP00000264079.5:n.681-101C>G
ENST00000394321.9:n.895C>G
ENST00000598406.1:n.636C>G
ENST00000601003.1:c.572-101C>G ENSP00000469074.1:n.572-101C>G
NM_020533.2:c.681-101C>G NP_065394.1:n.681-101C>G
NM_020533.3:c.681-101C>G MANE Select NP_065394.1:n.681-101C>G