Canonical Allele Identifier: CA2320965611
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022715371

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533885A>G , CM000681.2:g.7533885A>G GRCh38
NC_000019.9:g.7598771A>G , CM000681.1:g.7598771A>G GRCh37
NC_000019.8:g.7504771A>G NCBI36
NG_013374.1:g.4734A>G
NG_015806.1:g.16276A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*90A>G MANE Select ENSP00000264079.5:n.*90A>G
ENST00000264079.10:c.*90A>G ENSP00000264079.5:n.*90A>G
ENST00000394321.9:n.2148A>G
ENST00000599334.1:c.561A>G
ENST00000601870.1:c.169+17A>G
ENST00000602227.1:n.387A>G
NM_020533.2:c.*90A>G NP_065394.1:n.*90A>G
NM_020533.3:c.*90A>G MANE Select NP_065394.1:n.*90A>G