Canonical Allele Identifier: CA403089666
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530383G>C , CM000681.2:g.7530383G>C GRCh38
NC_000019.9:g.7595269G>C , CM000681.1:g.7595269G>C GRCh37
NC_000019.8:g.7501269G>C NCBI36
NG_013374.1:g.1232G>C
NG_015806.1:g.12774G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1457G>C MANE Select ENSP00000264079.5:p.Arg486Pro
ENST00000264079.10:c.1457G>C ENSP00000264079.5:p.Arg486Pro
ENST00000394321.9:n.1772G>C
ENST00000594692.1:n.453G>C
ENST00000595860.5:n.640G>C
ENST00000599334.1:c.237-52G>C
NM_020533.2:c.1457G>C NP_065394.1:p.Arg486Pro
NM_020533.3:c.1457G>C MANE Select NP_065394.1:p.Arg486Pro