Canonical Allele Identifier: CA403085723
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7593726G>T (hg19) chr19:g.7528840G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528840G>T , CM000681.2:g.7528840G>T GRCh38
NC_000019.9:g.7593726G>T , CM000681.1:g.7593726G>T GRCh37
NC_000019.8:g.7499726G>T NCBI36
NG_015806.1:g.11231G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1004G>T MANE Select ENSP00000264079.5:p.Trp335Leu
ENST00000264079.10:c.1004G>T ENSP00000264079.5:p.Trp335Leu
ENST00000394321.9:n.1319G>T
ENST00000595860.5:n.187G>T
NM_020533.2:c.1004G>T NP_065394.1:p.Trp335Leu
NM_020533.3:c.1004G>T MANE Select NP_065394.1:p.Trp335Leu
Search 100 bp 5'
Search 100 bp 3'