Canonical Allele Identifier: CA505226665
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7526507-A-G
MyVariant Identifiers: chr19:g.7591393A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526507A>G , CM000681.2:g.7526507A>G GRCh38
NC_000019.9:g.7591393A>G , CM000681.1:g.7591393A>G GRCh37
NC_000019.8:g.7497393A>G NCBI36
NG_015806.1:g.8898A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.306A>G MANE Select ENSP00000264079.5:p.Arg102=
ENST00000264079.10:c.306A>G ENSP00000264079.5:p.Arg102=
ENST00000394321.9:n.386A>G
ENST00000596008.1:n.268A>G
ENST00000598406.1:n.127A>G
ENST00000601003.1:c.306A>G ENSP00000469074.1:p.Arg102=
NM_020533.2:c.306A>G NP_065394.1:p.Arg102=
NM_020533.3:c.306A>G MANE Select NP_065394.1:p.Arg102=