Canonical Allele Identifier: CA403089033
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7530290-G-T

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1364G>T MANE Select ENSP00000264079.5:p.Arg455Leu
ENST00000264079.10:c.1364G>T ENSP00000264079.5:p.Arg455Leu
ENST00000394321.9:n.1679G>T
ENST00000594692.1:n.360G>T
ENST00000595860.5:n.547G>T
ENST00000599334.1:c.237-145G>T
NM_020533.2:c.1364G>T NP_065394.1:p.Arg455Leu
NM_020533.3:c.1364G>T MANE Select NP_065394.1:p.Arg455Leu