Canonical Allele Identifier: CA2320962311
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527467C= , CM000681.2:g.7527467C= GRCh38
NC_000019.9:g.7592353C= , CM000681.1:g.7592353C= GRCh37
NC_000019.8:g.7498353C= NCBI36
NG_015806.1:g.9858C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.572-53C= MANE Select ENSP00000264079.5:n.572-53C=
ENST00000264079.10:c.572-53C= ENSP00000264079.5:n.572-53C=
ENST00000394321.9:n.652-53C=
ENST00000598406.1:n.393-53C=
ENST00000601003.1:c.572-397C= ENSP00000469074.1:n.572-397C=
NM_020533.2:c.572-53C= NP_065394.1:n.572-53C=
NM_020533.3:c.572-53C= MANE Select NP_065394.1:n.572-53C=