Canonical Allele Identifier: CA2320962801

Gene: MCOLN1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7528423G= , CM000681.2:g.7528423G=	GRCh38
NC_000019.9:g.7593309G= , CM000681.1:g.7593309G=	GRCh37
NC_000019.8:g.7499309G=	NCBI36
NG_015806.1:g.10814G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.877+166G= MANE Select	ENSP00000264079.5:n.877+166G=
ENST00000264079.10:c.877+166G=	ENSP00000264079.5:n.877+166G=
ENST00000394321.9:n.1192+166G=
NM_020533.2:c.877+166G=	NP_065394.1:n.877+166G=
NM_020533.3:c.877+166G= MANE Select	NP_065394.1:n.877+166G=