Canonical Allele Identifier: CA2320961158
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525001C= , CM000681.2:g.7525001C= GRCh38
NC_000019.9:g.7589887C= , CM000681.1:g.7589887C= GRCh37
NC_000019.8:g.7495887C= NCBI36
NG_015806.1:g.7392C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.72C= MANE Select ENSP00000264079.5:p.Thr24=
ENST00000264079.10:c.72C= ENSP00000264079.5:p.Thr24=
ENST00000394321.9:n.152C=
ENST00000596390.1:n.188C=
ENST00000601003.1:c.72C= ENSP00000469074.1:p.Thr24=
NM_020533.2:c.72C= NP_065394.1:p.Thr24=
NM_020533.3:c.72C= MANE Select NP_065394.1:p.Thr24=