Canonical Allele Identifier: CA2587948324
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2146023391
gnomAD v4: 19-7527492-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527492A>G , CM000681.2:g.7527492A>G GRCh38
NC_000019.9:g.7592378A>G , CM000681.1:g.7592378A>G GRCh37
NC_000019.8:g.7498378A>G NCBI36
NG_015806.1:g.9883A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.572-28A>G MANE Select ENSP00000264079.5:n.572-28A>G
ENST00000264079.10:c.572-28A>G ENSP00000264079.5:n.572-28A>G
ENST00000394321.9:n.652-28A>G
ENST00000598406.1:n.393-28A>G
ENST00000601003.1:c.572-372A>G ENSP00000469074.1:n.572-372A>G
NM_020533.2:c.572-28A>G NP_065394.1:n.572-28A>G
NM_020533.3:c.572-28A>G MANE Select NP_065394.1:n.572-28A>G