Canonical Allele Identifier: CA2320962314
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527471C= , CM000681.2:g.7527471C= GRCh38
NC_000019.9:g.7592357C= , CM000681.1:g.7592357C= GRCh37
NC_000019.8:g.7498357C= NCBI36
NG_015806.1:g.9862C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.572-49C= MANE Select ENSP00000264079.5:n.572-49C=
ENST00000264079.10:c.572-49C= ENSP00000264079.5:n.572-49C=
ENST00000394321.9:n.652-49C=
ENST00000598406.1:n.393-49C=
ENST00000601003.1:c.572-393C= ENSP00000469074.1:n.572-393C=
NM_020533.2:c.572-49C= NP_065394.1:n.572-49C=
NM_020533.3:c.572-49C= MANE Select NP_065394.1:n.572-49C=