Canonical Allele Identifier: CA2587950418
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7533899-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533899G>A , CM000681.2:g.7533899G>A GRCh38
NC_000019.9:g.7598785G>A , CM000681.1:g.7598785G>A GRCh37
NC_000019.8:g.7504785G>A NCBI36
NG_013374.1:g.4748G>A
NG_015806.1:g.16290G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*104G>A MANE Select ENSP00000264079.5:n.*104G>A
ENST00000264079.10:c.*104G>A ENSP00000264079.5:n.*104G>A
ENST00000394321.9:n.2162G>A
ENST00000599334.1:c.575G>A
ENST00000601870.1:c.169+31G>A
ENST00000602227.1:n.401G>A
NM_020533.2:c.*104G>A NP_065394.1:n.*104G>A
NM_020533.3:c.*104G>A MANE Select NP_065394.1:n.*104G>A