Canonical Allele Identifier: CA2587950377
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7533803-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533803T>A , CM000681.2:g.7533803T>A GRCh38
NC_000019.9:g.7598689T>A , CM000681.1:g.7598689T>A GRCh37
NC_000019.8:g.7504689T>A NCBI36
NG_013374.1:g.4652T>A
NG_015806.1:g.16194T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*8T>A MANE Select ENSP00000264079.5:n.*8T>A
ENST00000264079.10:c.*8T>A ENSP00000264079.5:n.*8T>A
ENST00000394321.9:n.2066T>A
ENST00000599334.1:c.479T>A
ENST00000601870.1:c.104T>A
ENST00000602227.1:n.305T>A
NM_020533.2:c.*8T>A NP_065394.1:n.*8T>A
NM_020533.3:c.*8T>A MANE Select NP_065394.1:n.*8T>A