Canonical Allele Identifier: CA403085397
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7593542T>G (hg19) chr19:g.7528656T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528656T>G , CM000681.2:g.7528656T>G GRCh38
NC_000019.9:g.7593542T>G , CM000681.1:g.7593542T>G GRCh37
NC_000019.8:g.7499542T>G NCBI36
NG_015806.1:g.11047T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.937T>G MANE Select ENSP00000264079.5:p.Phe313Val
ENST00000264079.10:c.937T>G ENSP00000264079.5:p.Phe313Val
ENST00000394321.9:n.1252T>G
ENST00000595860.5:n.3T>G
NM_020533.2:c.937T>G NP_065394.1:p.Phe313Val
NM_020533.3:c.937T>G MANE Select NP_065394.1:p.Phe313Val
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Search 100 bp 3'