Canonical Allele Identifier: CA2320963541
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022629831
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529904T>A , CM000681.2:g.7529904T>A GRCh38
NC_000019.9:g.7594790T>A , CM000681.1:g.7594790T>A GRCh37
NC_000019.8:g.7500790T>A NCBI36
NG_013374.1:g.753T>A
NG_015806.1:g.12295T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1359+192T>A MANE Select ENSP00000264079.5:n.1359+192T>A
ENST00000264079.10:c.1359+192T>A ENSP00000264079.5:n.1359+192T>A
ENST00000394321.9:n.1674+192T>A
ENST00000594692.1:n.355+192T>A
ENST00000595860.5:n.542+192T>A
ENST00000599334.1:c.236+192T>A
NM_020533.2:c.1359+192T>A NP_065394.1:n.1359+192T>A
NM_020533.3:c.1359+192T>A MANE Select NP_065394.1:n.1359+192T>A
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