Canonical Allele Identifier: CA2587946797
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7525214-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525214C>A , CM000681.2:g.7525214C>A GRCh38
NC_000019.9:g.7590100C>A , CM000681.1:g.7590100C>A GRCh37
NC_000019.8:g.7496100C>A NCBI36
NG_015806.1:g.7605C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.237+48C>A MANE Select ENSP00000264079.5:n.237+48C>A
ENST00000264079.10:c.237+48C>A ENSP00000264079.5:n.237+48C>A
ENST00000394321.9:n.317+48C>A
ENST00000596390.1:n.401C>A
ENST00000601003.1:c.237+48C>A ENSP00000469074.1:n.237+48C>A
NM_020533.2:c.237+48C>A NP_065394.1:n.237+48C>A
NM_020533.3:c.237+48C>A MANE Select NP_065394.1:n.237+48C>A