Canonical Allele Identifier: CA403087644
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529639G>A , CM000681.2:g.7529639G>A GRCh38
NC_000019.9:g.7594525G>A , CM000681.1:g.7594525G>A GRCh37
NC_000019.8:g.7500525G>A NCBI36
NG_013374.1:g.488G>A
NG_015806.1:g.12030G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1286G>A MANE Select ENSP00000264079.5:p.Cys429Tyr
ENST00000264079.10:c.1286G>A ENSP00000264079.5:p.Cys429Tyr
ENST00000394321.9:n.1601G>A
ENST00000594692.1:n.282G>A
ENST00000595860.5:n.469G>A
ENST00000599334.1:c.163G>A
NM_020533.2:c.1286G>A NP_065394.1:p.Cys429Tyr
NM_020533.3:c.1286G>A MANE Select NP_065394.1:p.Cys429Tyr