Canonical Allele Identifier: CA403088132
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7594587T>A (hg19) chr19:g.7529701T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529701T>A , CM000681.2:g.7529701T>A GRCh38
NC_000019.9:g.7594587T>A , CM000681.1:g.7594587T>A GRCh37
NC_000019.8:g.7500587T>A NCBI36
NG_013374.1:g.550T>A
NG_015806.1:g.12092T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1348T>A MANE Select ENSP00000264079.5:p.Tyr450Asn
ENST00000264079.10:c.1348T>A ENSP00000264079.5:p.Tyr450Asn
ENST00000394321.9:n.1663T>A
ENST00000594692.1:n.344T>A
ENST00000595860.5:n.531T>A
ENST00000599334.1:c.225T>A
NM_020533.2:c.1348T>A NP_065394.1:p.Tyr450Asn
NM_020533.3:c.1348T>A MANE Select NP_065394.1:p.Tyr450Asn
Search 100 bp 5'
Search 100 bp 3'