Canonical Allele Identifier: CA403089673
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022638713
gnomAD v3: 19-7530385-A-G
gnomAD v4: 19-7530385-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530385A>G , CM000681.2:g.7530385A>G GRCh38
NC_000019.9:g.7595271A>G , CM000681.1:g.7595271A>G GRCh37
NC_000019.8:g.7501271A>G NCBI36
NG_013374.1:g.1234A>G
NG_015806.1:g.12776A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1459A>G MANE Select ENSP00000264079.5:p.Ser487Gly
ENST00000264079.10:c.1459A>G ENSP00000264079.5:p.Ser487Gly
ENST00000394321.9:n.1774A>G
ENST00000594692.1:n.455A>G
ENST00000595860.5:n.642A>G
ENST00000599334.1:c.237-50A>G
NM_020533.2:c.1459A>G NP_065394.1:p.Ser487Gly
NM_020533.3:c.1459A>G MANE Select NP_065394.1:p.Ser487Gly