Canonical Allele Identifier: CA403088007

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7594566G>A (hg19) ; chr19:g.7529680G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7529680G>A , CM000681.2:g.7529680G>A	GRCh38
NC_000019.9:g.7594566G>A , CM000681.1:g.7594566G>A	GRCh37
NC_000019.8:g.7500566G>A	NCBI36
NG_013374.1:g.529G>A
NG_015806.1:g.12071G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.1327G>A MANE Select	ENSP00000264079.5:p.Gly443Ser
ENST00000264079.10:c.1327G>A	ENSP00000264079.5:p.Gly443Ser
ENST00000394321.9:n.1642G>A
ENST00000594692.1:n.323G>A
ENST00000595860.5:n.510G>A
ENST00000599334.1:c.204G>A
NM_020533.2:c.1327G>A	NP_065394.1:p.Gly443Ser
NM_020533.3:c.1327G>A MANE Select	NP_065394.1:p.Gly443Ser