Canonical Allele Identifier: CA505233416
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7598537A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533651A>G , CM000681.2:g.7533651A>G GRCh38
NC_000019.9:g.7598537A>G , CM000681.1:g.7598537A>G GRCh37
NC_000019.8:g.7504537A>G NCBI36
NG_013374.1:g.4500A>G
NG_015806.1:g.16042A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1704A>G MANE Select ENSP00000264079.5:p.Gly568=
ENST00000264079.10:c.1704A>G ENSP00000264079.5:p.Gly568=
ENST00000394321.9:n.2019A>G
ENST00000599334.1:c.432A>G
ENST00000601870.1:c.57A>G
ENST00000602227.1:n.258A>G
NM_020533.2:c.1704A>G NP_065394.1:p.Gly568=
NM_020533.3:c.1704A>G MANE Select NP_065394.1:p.Gly568=