Canonical Allele Identifier: CA2587950337
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7533501-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533501G>A , CM000681.2:g.7533501G>A GRCh38
NC_000019.9:g.7598387G>A , CM000681.1:g.7598387G>A GRCh37
NC_000019.8:g.7504387G>A NCBI36
NG_013374.1:g.4350G>A
NG_015806.1:g.15892G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1576-22G>A MANE Select ENSP00000264079.5:n.1576-22G>A
ENST00000264079.10:c.1576-22G>A ENSP00000264079.5:n.1576-22G>A
ENST00000394321.9:n.1891-22G>A
ENST00000599334.1:c.304-22G>A
ENST00000602227.1:n.108G>A
NM_020533.2:c.1576-22G>A NP_065394.1:n.1576-22G>A
NM_020533.3:c.1576-22G>A MANE Select NP_065394.1:n.1576-22G>A