Canonical Allele Identifier: CA2587948302
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7527473-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527473T>A , CM000681.2:g.7527473T>A GRCh38
NC_000019.9:g.7592359T>A , CM000681.1:g.7592359T>A GRCh37
NC_000019.8:g.7498359T>A NCBI36
NG_015806.1:g.9864T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.572-47T>A MANE Select ENSP00000264079.5:n.572-47T>A
ENST00000264079.10:c.572-47T>A ENSP00000264079.5:n.572-47T>A
ENST00000394321.9:n.652-47T>A
ENST00000598406.1:n.393-47T>A
ENST00000601003.1:c.572-391T>A ENSP00000469074.1:n.572-391T>A
NM_020533.2:c.572-47T>A NP_065394.1:n.572-47T>A
NM_020533.3:c.572-47T>A MANE Select NP_065394.1:n.572-47T>A
Search 100 bp 5'
Search 100 bp 3'