Canonical Allele Identifier: CA403089618
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7530376-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530376C>G , CM000681.2:g.7530376C>G GRCh38
NC_000019.9:g.7595262C>G , CM000681.1:g.7595262C>G GRCh37
NC_000019.8:g.7501262C>G NCBI36
NG_013374.1:g.1225C>G
NG_015806.1:g.12767C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1450C>G MANE Select ENSP00000264079.5:p.Gln484Glu
ENST00000264079.10:c.1450C>G ENSP00000264079.5:p.Gln484Glu
ENST00000394321.9:n.1765C>G
ENST00000594692.1:n.446C>G
ENST00000595860.5:n.633C>G
ENST00000599334.1:c.237-59C>G
NM_020533.2:c.1450C>G NP_065394.1:p.Gln484Glu
NM_020533.3:c.1450C>G MANE Select NP_065394.1:p.Gln484Glu