Canonical Allele Identifier: CA403089036
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530290G>C , CM000681.2:g.7530290G>C GRCh38
NC_000019.9:g.7595176G>C , CM000681.1:g.7595176G>C GRCh37
NC_000019.8:g.7501176G>C NCBI36
NG_013374.1:g.1139G>C
NG_015806.1:g.12681G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1364G>C MANE Select ENSP00000264079.5:p.Arg455Pro
ENST00000264079.10:c.1364G>C ENSP00000264079.5:p.Arg455Pro
ENST00000394321.9:n.1679G>C
ENST00000594692.1:n.360G>C
ENST00000595860.5:n.547G>C
ENST00000599334.1:c.237-145G>C
NM_020533.2:c.1364G>C NP_065394.1:p.Arg455Pro
NM_020533.3:c.1364G>C MANE Select NP_065394.1:p.Arg455Pro