Canonical Allele Identifier: CA2320963584
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022631000
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529981A>C , CM000681.2:g.7529981A>C GRCh38
NC_000019.9:g.7594867A>C , CM000681.1:g.7594867A>C GRCh37
NC_000019.8:g.7500867A>C NCBI36
NG_013374.1:g.830A>C
NG_015806.1:g.12372A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1359+269A>C MANE Select ENSP00000264079.5:n.1359+269A>C
ENST00000264079.10:c.1359+269A>C ENSP00000264079.5:n.1359+269A>C
ENST00000394321.9:n.1674+269A>C
ENST00000594692.1:n.355+269A>C
ENST00000595860.5:n.542+269A>C
ENST00000599334.1:c.236+269A>C
NM_020533.2:c.1359+269A>C NP_065394.1:n.1359+269A>C
NM_020533.3:c.1359+269A>C MANE Select NP_065394.1:n.1359+269A>C
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