Canonical Allele Identifier: CA403152343
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7589854G>C (hg19) chr19:g.7524968G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7524968G>C , CM000681.2:g.7524968G>C GRCh38
NC_000019.9:g.7589854G>C , CM000681.1:g.7589854G>C GRCh37
NC_000019.8:g.7495854G>C NCBI36
NG_015806.1:g.7359G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.39G>C MANE Select ENSP00000264079.5:p.Glu13Asp
ENST00000264079.10:c.39G>C ENSP00000264079.5:p.Glu13Asp
ENST00000394321.9:n.119G>C
ENST00000596390.1:n.155G>C
ENST00000601003.1:c.39G>C ENSP00000469074.1:p.Glu13Asp
NM_020533.2:c.39G>C NP_065394.1:p.Glu13Asp
XR_936293.2:n.13C>G
XR_936294.2:n.13C>G
NM_020533.3:c.39G>C MANE Select NP_065394.1:p.Glu13Asp
Search 100 bp 5'
Search 100 bp 3'