Canonical Allele Identifier: CA403091862

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7598532T>A (hg19) ; chr19:g.7533646T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7533646T>A , CM000681.2:g.7533646T>A	GRCh38
NC_000019.9:g.7598532T>A , CM000681.1:g.7598532T>A	GRCh37
NC_000019.8:g.7504532T>A	NCBI36
NG_013374.1:g.4495T>A
NG_015806.1:g.16037T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.1699T>A MANE Select	ENSP00000264079.5:p.Cys567Ser
ENST00000264079.10:c.1699T>A	ENSP00000264079.5:p.Cys567Ser
ENST00000394321.9:n.2014T>A
ENST00000599334.1:c.427T>A
ENST00000601870.1:c.52T>A
ENST00000602227.1:n.253T>A
NM_020533.2:c.1699T>A	NP_065394.1:p.Cys567Ser
NM_020533.3:c.1699T>A MANE Select	NP_065394.1:p.Cys567Ser