Canonical Allele Identifier: CA2320962298

Gene: MCOLN1

Linked Data

• dbSNP Id: rs1792891465

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7527420A>G , CM000681.2:g.7527420A>G	GRCh38
NC_000019.9:g.7592306A>G , CM000681.1:g.7592306A>G	GRCh37
NC_000019.8:g.7498306A>G	NCBI36
NG_015806.1:g.9811A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264079.11:c.572-100A>G MANE Select	ENSP00000264079.5:n.572-100A>G
ENST00000264079.10:c.572-100A>G	ENSP00000264079.5:n.572-100A>G
ENST00000394321.9:n.652-100A>G
ENST00000598406.1:n.393-100A>G
ENST00000601003.1:c.572-444A>G	ENSP00000469074.1:n.572-444A>G
NM_020533.2:c.572-100A>G	NP_065394.1:n.572-100A>G
NM_020533.3:c.572-100A>G MANE Select	NP_065394.1:n.572-100A>G