Canonical Allele Identifier: CA2587946743
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7524889-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7524889C>A , CM000681.2:g.7524889C>A GRCh38
NC_000019.9:g.7589775C>A , CM000681.1:g.7589775C>A GRCh37
NC_000019.8:g.7495775C>A NCBI36
NG_015806.1:g.7280C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.32-72C>A MANE Select ENSP00000264079.5:n.32-72C>A
ENST00000264079.10:c.32-72C>A ENSP00000264079.5:n.32-72C>A
ENST00000394321.9:n.112-72C>A
ENST00000596390.1:n.148-72C>A
ENST00000601003.1:c.32-72C>A ENSP00000469074.1:n.32-72C>A
NM_020533.2:c.32-72C>A NP_065394.1:n.32-72C>A
XR_936293.1:n.66G>T
XR_936294.1:n.66G>T
XR_936295.1:n.66G>T
XR_936293.2:n.92G>T
XR_936294.2:n.92G>T
NM_020533.3:c.32-72C>A MANE Select NP_065394.1:n.32-72C>A