Canonical Allele Identifier: CA2320965655
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022718760
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533967G>A , CM000681.2:g.7533967G>A GRCh38
NC_000019.9:g.7598853G>A , CM000681.1:g.7598853G>A GRCh37
NC_000019.8:g.7504853G>A NCBI36
NG_013374.1:g.4816G>A
NG_015806.1:g.16358G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*172G>A MANE Select ENSP00000264079.5:n.*172G>A
ENST00000264079.10:c.*172G>A ENSP00000264079.5:n.*172G>A
ENST00000394321.9:n.2230G>A
ENST00000599334.1:c.643G>A
ENST00000601870.1:c.169+99G>A
ENST00000602227.1:n.469G>A
NM_020533.2:c.*172G>A NP_065394.1:n.*172G>A
NM_020533.3:c.*172G>A MANE Select NP_065394.1:n.*172G>A
Search 100 bp 5'
Search 100 bp 3'