Canonical Allele Identifier: CA505233360
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7533576-G-A
MyVariant Identifiers: chr19:g.7598462G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533576G>A , CM000681.2:g.7533576G>A GRCh38
NC_000019.9:g.7598462G>A , CM000681.1:g.7598462G>A GRCh37
NC_000019.8:g.7504462G>A NCBI36
NG_013374.1:g.4425G>A
NG_015806.1:g.15967G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1629G>A MANE Select ENSP00000264079.5:p.Gln543=
ENST00000264079.10:c.1629G>A ENSP00000264079.5:p.Gln543=
ENST00000394321.9:n.1944G>A
ENST00000599334.1:c.357G>A
ENST00000602227.1:n.183G>A
NM_020533.2:c.1629G>A NP_065394.1:p.Gln543=
NM_020533.3:c.1629G>A MANE Select NP_065394.1:p.Gln543=