Canonical Allele Identifier: CA2587947888
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7526680-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526680T>A , CM000681.2:g.7526680T>A GRCh38
NC_000019.9:g.7591566T>A , CM000681.1:g.7591566T>A GRCh37
NC_000019.8:g.7497566T>A NCBI36
NG_015806.1:g.9071T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.405+74T>A MANE Select ENSP00000264079.5:n.405+74T>A
ENST00000264079.10:c.405+74T>A ENSP00000264079.5:n.405+74T>A
ENST00000394321.9:n.485+74T>A
ENST00000596008.1:n.367+74T>A
ENST00000598406.1:n.226+74T>A
ENST00000601003.1:c.405+74T>A ENSP00000469074.1:n.405+74T>A
NM_020533.2:c.405+74T>A NP_065394.1:n.405+74T>A
NM_020533.3:c.405+74T>A MANE Select NP_065394.1:n.405+74T>A