Canonical Allele Identifier: CA403091541
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533579C>G , CM000681.2:g.7533579C>G GRCh38
NC_000019.9:g.7598465C>G , CM000681.1:g.7598465C>G GRCh37
NC_000019.8:g.7504465C>G NCBI36
NG_013374.1:g.4428C>G
NG_015806.1:g.15970C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1632C>G MANE Select ENSP00000264079.5:p.Cys544Trp
ENST00000264079.10:c.1632C>G ENSP00000264079.5:p.Cys544Trp
ENST00000394321.9:n.1947C>G
ENST00000599334.1:c.360C>G
ENST00000602227.1:n.186C>G
NM_020533.2:c.1632C>G NP_065394.1:p.Cys544Trp
NM_020533.3:c.1632C>G MANE Select NP_065394.1:p.Cys544Trp