Canonical Allele Identifier: CA403088307
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7594598G>C (hg19) chr19:g.7529712G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529712G>C , CM000681.2:g.7529712G>C GRCh38
NC_000019.9:g.7594598G>C , CM000681.1:g.7594598G>C GRCh37
NC_000019.8:g.7500598G>C NCBI36
NG_013374.1:g.561G>C
NG_015806.1:g.12103G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1359G>C MANE Select ENSP00000264079.5:p.Lys453Asn
ENST00000264079.10:c.1359G>C ENSP00000264079.5:p.Lys453Asn
ENST00000394321.9:n.1674G>C
ENST00000594692.1:n.355G>C
ENST00000595860.5:n.542G>C
ENST00000599334.1:c.236G>C
NM_020533.2:c.1359G>C NP_065394.1:p.Lys453Asn
NM_020533.3:c.1359G>C MANE Select NP_065394.1:p.Lys453Asn
Search 100 bp 5'
Search 100 bp 3'