Canonical Allele Identifier: CA2735602236
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2146030829

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533863T>G , CM000681.2:g.7533863T>G GRCh38
NC_000019.9:g.7598749T>G , CM000681.1:g.7598749T>G GRCh37
NC_000019.8:g.7504749T>G NCBI36
NG_013374.1:g.4712T>G
NG_015806.1:g.16254T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*68T>G MANE Select ENSP00000264079.5:n.*68T>G
ENST00000264079.10:c.*68T>G ENSP00000264079.5:n.*68T>G
ENST00000394321.9:n.2126T>G
ENST00000599334.1:c.539T>G
ENST00000601870.1:c.164T>G
ENST00000602227.1:n.365T>G
NM_020533.2:c.*68T>G NP_065394.1:n.*68T>G
NM_020533.3:c.*68T>G MANE Select NP_065394.1:n.*68T>G