Canonical Allele Identifier: CA403082129
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7527564-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527564A>G , CM000681.2:g.7527564A>G GRCh38
NC_000019.9:g.7592450A>G , CM000681.1:g.7592450A>G GRCh37
NC_000019.8:g.7498450A>G NCBI36
NG_015806.1:g.9955A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.616A>G MANE Select ENSP00000264079.5:p.Ser206Gly
ENST00000264079.10:c.616A>G ENSP00000264079.5:p.Ser206Gly
ENST00000394321.9:n.696A>G
ENST00000598406.1:n.437A>G
ENST00000601003.1:c.572-300A>G ENSP00000469074.1:n.572-300A>G
NM_020533.2:c.616A>G NP_065394.1:p.Ser206Gly
NM_020533.3:c.616A>G MANE Select NP_065394.1:p.Ser206Gly