Canonical Allele Identifier: CA2587946694
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7524835-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7524835T>C , CM000681.2:g.7524835T>C GRCh38
NC_000019.9:g.7589721T>C , CM000681.1:g.7589721T>C GRCh37
NC_000019.8:g.7495721T>C NCBI36
NG_015806.1:g.7226T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.32-126T>C MANE Select ENSP00000264079.5:n.32-126T>C
ENST00000264079.10:c.32-126T>C ENSP00000264079.5:n.32-126T>C
ENST00000394321.9:n.112-126T>C
ENST00000596390.1:n.148-126T>C
ENST00000601003.1:c.32-126T>C ENSP00000469074.1:n.32-126T>C
NM_020533.2:c.32-126T>C NP_065394.1:n.32-126T>C
XR_936293.1:n.120A>G
XR_936294.1:n.120A>G
XR_936295.1:n.120A>G
XR_936293.2:n.146A>G
XR_936294.2:n.146A>G
NM_020533.3:c.32-126T>C MANE Select NP_065394.1:n.32-126T>C