Canonical Allele Identifier: CA2320962173

Gene: MCOLN1

Linked Data

• dbSNP Id: rs2022583805

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7527192A>C , CM000681.2:g.7527192A>C	GRCh38
NC_000019.9:g.7592078A>C , CM000681.1:g.7592078A>C	GRCh37
NC_000019.8:g.7498078A>C	NCBI36
NG_015806.1:g.9583A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.571+266A>C MANE Select	ENSP00000264079.5:n.571+266A>C
ENST00000264079.10:c.571+266A>C	ENSP00000264079.5:n.571+266A>C
ENST00000394321.9:n.651+266A>C
ENST00000598406.1:n.392+266A>C
ENST00000601003.1:c.571+266A>C	ENSP00000469074.1:n.571+266A>C
NM_020533.2:c.571+266A>C	NP_065394.1:n.571+266A>C
NM_020533.3:c.571+266A>C MANE Select	NP_065394.1:n.571+266A>C