Canonical Allele Identifier: CA2320962597
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527980C= , CM000681.2:g.7527980C= GRCh38
NC_000019.9:g.7592866C= , CM000681.1:g.7592866C= GRCh37
NC_000019.8:g.7498866C= NCBI36
NG_015806.1:g.10371C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.777+20C= MANE Select ENSP00000264079.5:n.777+20C=
ENST00000264079.10:c.777+20C= ENSP00000264079.5:n.777+20C=
ENST00000394321.9:n.1092+20C=
NM_020533.2:c.777+20C= NP_065394.1:n.777+20C=
NM_020533.3:c.777+20C= MANE Select NP_065394.1:n.777+20C=