Canonical Allele Identifier: CA2587946697
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7524837-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7524837A>C , CM000681.2:g.7524837A>C GRCh38
NC_000019.9:g.7589723A>C , CM000681.1:g.7589723A>C GRCh37
NC_000019.8:g.7495723A>C NCBI36
NG_015806.1:g.7228A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.32-124A>C MANE Select ENSP00000264079.5:n.32-124A>C
ENST00000264079.10:c.32-124A>C ENSP00000264079.5:n.32-124A>C
ENST00000394321.9:n.112-124A>C
ENST00000596390.1:n.148-124A>C
ENST00000601003.1:c.32-124A>C ENSP00000469074.1:n.32-124A>C
NM_020533.2:c.32-124A>C NP_065394.1:n.32-124A>C
XR_936293.1:n.118T>G
XR_936294.1:n.118T>G
XR_936295.1:n.118T>G
XR_936293.2:n.144T>G
XR_936294.2:n.144T>G
NM_020533.3:c.32-124A>C MANE Select NP_065394.1:n.32-124A>C