Canonical Allele Identifier: CA2320962809

Gene: MCOLN1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7528442C= , CM000681.2:g.7528442C=	GRCh38
NC_000019.9:g.7593328C= , CM000681.1:g.7593328C=	GRCh37
NC_000019.8:g.7499328C=	NCBI36
NG_015806.1:g.10833C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.878-155C= MANE Select	ENSP00000264079.5:n.878-155C=
ENST00000264079.10:c.878-155C=	ENSP00000264079.5:n.878-155C=
ENST00000394321.9:n.1193-155C=
NM_020533.2:c.878-155C=	NP_065394.1:n.878-155C=
NM_020533.3:c.878-155C= MANE Select	NP_065394.1:n.878-155C=