Canonical Allele Identifier: CA403091568
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7598471C>G (hg19) chr19:g.7533585C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533585C>G , CM000681.2:g.7533585C>G GRCh38
NC_000019.9:g.7598471C>G , CM000681.1:g.7598471C>G GRCh37
NC_000019.8:g.7504471C>G NCBI36
NG_013374.1:g.4434C>G
NG_015806.1:g.15976C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1638C>G MANE Select ENSP00000264079.5:p.Asp546Glu
ENST00000264079.10:c.1638C>G ENSP00000264079.5:p.Asp546Glu
ENST00000394321.9:n.1953C>G
ENST00000599334.1:c.366C>G
ENST00000602227.1:n.192C>G
NM_020533.2:c.1638C>G NP_065394.1:p.Asp546Glu
NM_020533.3:c.1638C>G MANE Select NP_065394.1:p.Asp546Glu
Search 100 bp 5'
Search 100 bp 3'