Canonical Allele Identifier: CA403091535
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533578G>C , CM000681.2:g.7533578G>C GRCh38
NC_000019.9:g.7598464G>C , CM000681.1:g.7598464G>C GRCh37
NC_000019.8:g.7504464G>C NCBI36
NG_013374.1:g.4427G>C
NG_015806.1:g.15969G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1631G>C MANE Select ENSP00000264079.5:p.Cys544Ser
ENST00000264079.10:c.1631G>C ENSP00000264079.5:p.Cys544Ser
ENST00000394321.9:n.1946G>C
ENST00000599334.1:c.359G>C
ENST00000602227.1:n.185G>C
NM_020533.2:c.1631G>C NP_065394.1:p.Cys544Ser
NM_020533.3:c.1631G>C MANE Select NP_065394.1:p.Cys544Ser