Canonical Allele Identifier: CA403084355

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7592845T>G (hg19) ; chr19:g.7527959T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7527959T>G , CM000681.2:g.7527959T>G	GRCh38
NC_000019.9:g.7592845T>G , CM000681.1:g.7592845T>G	GRCh37
NC_000019.8:g.7498845T>G	NCBI36
NG_015806.1:g.10350T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.776T>G MANE Select	ENSP00000264079.5:p.Leu259Arg
ENST00000264079.10:c.776T>G	ENSP00000264079.5:p.Leu259Arg
ENST00000394321.9:n.1091T>G
NM_020533.2:c.776T>G	NP_065394.1:p.Leu259Arg
NM_020533.3:c.776T>G MANE Select	NP_065394.1:p.Leu259Arg