Canonical Allele Identifier: CA2739637990
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527844C>G , CM000681.2:g.7527844C>G GRCh38
NC_000019.9:g.7592730C>G , CM000681.1:g.7592730C>G GRCh37
NC_000019.8:g.7498730C>G NCBI36
NG_015806.1:g.10235C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-20C>G MANE Select ENSP00000264079.5:n.681-20C>G
ENST00000264079.10:c.681-20C>G ENSP00000264079.5:n.681-20C>G
ENST00000394321.9:n.976C>G
ENST00000601003.1:c.572-20C>G ENSP00000469074.1:n.572-20C>G
NM_020533.2:c.681-20C>G NP_065394.1:n.681-20C>G
NM_020533.3:c.681-20C>G MANE Select NP_065394.1:n.681-20C>G