Canonical Allele Identifier: CA403091523
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7533576-G-C

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1629G>C MANE Select ENSP00000264079.5:p.Gln543His
ENST00000264079.10:c.1629G>C ENSP00000264079.5:p.Gln543His
ENST00000394321.9:n.1944G>C
ENST00000599334.1:c.357G>C
ENST00000602227.1:n.183G>C
NM_020533.2:c.1629G>C NP_065394.1:p.Gln543His
NM_020533.3:c.1629G>C MANE Select NP_065394.1:p.Gln543His