Canonical Allele Identifier: CA2587948109
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7527215-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527215T>G , CM000681.2:g.7527215T>G GRCh38
NC_000019.9:g.7592101T>G , CM000681.1:g.7592101T>G GRCh37
NC_000019.8:g.7498101T>G NCBI36
NG_015806.1:g.9606T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.571+289T>G MANE Select ENSP00000264079.5:n.571+289T>G
ENST00000264079.10:c.571+289T>G ENSP00000264079.5:n.571+289T>G
ENST00000394321.9:n.651+289T>G
ENST00000598406.1:n.392+289T>G
ENST00000601003.1:c.571+289T>G ENSP00000469074.1:n.571+289T>G
NM_020533.2:c.571+289T>G NP_065394.1:n.571+289T>G
NM_020533.3:c.571+289T>G MANE Select NP_065394.1:n.571+289T>G
Search 100 bp 5'
Search 100 bp 3'