Canonical Allele Identifier: CA2576597034
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7528079-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528079G>A , CM000681.2:g.7528079G>A GRCh38
NC_000019.9:g.7592965G>A , CM000681.1:g.7592965G>A GRCh37
NC_000019.8:g.7498965G>A NCBI36
NG_015806.1:g.10470G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.778-79G>A MANE Select ENSP00000264079.5:n.778-79G>A
ENST00000264079.10:c.778-79G>A ENSP00000264079.5:n.778-79G>A
ENST00000394321.9:n.1093-79G>A
NM_020533.2:c.778-79G>A NP_065394.1:n.778-79G>A
NM_020533.3:c.778-79G>A MANE Select NP_065394.1:n.778-79G>A
Search 100 bp 5'
Search 100 bp 3'