Canonical Allele Identifier: CA403091562
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7598470A>C (hg19) chr19:g.7533584A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533584A>C , CM000681.2:g.7533584A>C GRCh38
NC_000019.9:g.7598470A>C , CM000681.1:g.7598470A>C GRCh37
NC_000019.8:g.7504470A>C NCBI36
NG_013374.1:g.4433A>C
NG_015806.1:g.15975A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1637A>C MANE Select ENSP00000264079.5:p.Asp546Ala
ENST00000264079.10:c.1637A>C ENSP00000264079.5:p.Asp546Ala
ENST00000394321.9:n.1952A>C
ENST00000599334.1:c.365A>C
ENST00000602227.1:n.191A>C
NM_020533.2:c.1637A>C NP_065394.1:p.Asp546Ala
NM_020533.3:c.1637A>C MANE Select NP_065394.1:p.Asp546Ala
Search 100 bp 5'
Search 100 bp 3'