Canonical Allele Identifier: CA2587947825
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7526355-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526355G>A , CM000681.2:g.7526355G>A GRCh38
NC_000019.9:g.7591241G>A , CM000681.1:g.7591241G>A GRCh37
NC_000019.8:g.7497241G>A NCBI36
NG_015806.1:g.8746G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.238-84G>A MANE Select ENSP00000264079.5:n.238-84G>A
ENST00000264079.10:c.238-84G>A ENSP00000264079.5:n.238-84G>A
ENST00000394321.9:n.318-84G>A
ENST00000596008.1:n.116G>A
ENST00000601003.1:c.238-84G>A ENSP00000469074.1:n.238-84G>A
NM_020533.2:c.238-84G>A NP_065394.1:n.238-84G>A
NM_020533.3:c.238-84G>A MANE Select NP_065394.1:n.238-84G>A