Canonical Allele Identifier: CA403085304

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7593522T>G (hg19) ; chr19:g.7528636T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7528636T>G , CM000681.2:g.7528636T>G	GRCh38
NC_000019.9:g.7593522T>G , CM000681.1:g.7593522T>G	GRCh37
NC_000019.8:g.7499522T>G	NCBI36
NG_015806.1:g.11027T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.917T>G MANE Select	ENSP00000264079.5:p.Ile306Ser
ENST00000264079.10:c.917T>G	ENSP00000264079.5:p.Ile306Ser
ENST00000394321.9:n.1232T>G
NM_020533.2:c.917T>G	NP_065394.1:p.Ile306Ser
NM_020533.3:c.917T>G MANE Select	NP_065394.1:p.Ile306Ser