Canonical Allele Identifier: CA403086239
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528935T>G , CM000681.2:g.7528935T>G GRCh38
NC_000019.9:g.7593821T>G , CM000681.1:g.7593821T>G GRCh37
NC_000019.8:g.7499821T>G NCBI36
NG_015806.1:g.11326T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1099T>G MANE Select ENSP00000264079.5:p.Ser367Ala
ENST00000264079.10:c.1099T>G ENSP00000264079.5:p.Ser367Ala
ENST00000394321.9:n.1414T>G
ENST00000595860.5:n.282T>G
NM_020533.2:c.1099T>G NP_065394.1:p.Ser367Ala
NM_020533.3:c.1099T>G MANE Select NP_065394.1:p.Ser367Ala