Canonical Allele Identifier: CA403088176
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529702A>G , CM000681.2:g.7529702A>G GRCh38
NC_000019.9:g.7594588A>G , CM000681.1:g.7594588A>G GRCh37
NC_000019.8:g.7500588A>G NCBI36
NG_013374.1:g.551A>G
NG_015806.1:g.12093A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1349A>G MANE Select ENSP00000264079.5:p.Tyr450Cys
ENST00000264079.10:c.1349A>G ENSP00000264079.5:p.Tyr450Cys
ENST00000394321.9:n.1664A>G
ENST00000594692.1:n.345A>G
ENST00000595860.5:n.532A>G
ENST00000599334.1:c.226A>G
NM_020533.2:c.1349A>G NP_065394.1:p.Tyr450Cys
NM_020533.3:c.1349A>G MANE Select NP_065394.1:p.Tyr450Cys