Canonical Allele Identifier: CA403082278
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527589G>C , CM000681.2:g.7527589G>C GRCh38
NC_000019.9:g.7592475G>C , CM000681.1:g.7592475G>C GRCh37
NC_000019.8:g.7498475G>C NCBI36
NG_015806.1:g.9980G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.641G>C MANE Select ENSP00000264079.5:p.Ser214Thr
ENST00000264079.10:c.641G>C ENSP00000264079.5:p.Ser214Thr
ENST00000394321.9:n.721G>C
ENST00000598406.1:n.462G>C
ENST00000601003.1:c.572-275G>C ENSP00000469074.1:n.572-275G>C
NM_020533.2:c.641G>C NP_065394.1:p.Ser214Thr
NM_020533.3:c.641G>C MANE Select NP_065394.1:p.Ser214Thr