Canonical Allele Identifier: CA2587948362
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7527651-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527651G>A , CM000681.2:g.7527651G>A GRCh38
NC_000019.9:g.7592537G>A , CM000681.1:g.7592537G>A GRCh37
NC_000019.8:g.7498537G>A NCBI36
NG_015806.1:g.10042G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.680+23G>A MANE Select ENSP00000264079.5:n.680+23G>A
ENST00000264079.10:c.680+23G>A ENSP00000264079.5:n.680+23G>A
ENST00000394321.9:n.783G>A
ENST00000598406.1:n.524G>A
ENST00000601003.1:c.572-213G>A ENSP00000469074.1:n.572-213G>A
NM_020533.2:c.680+23G>A NP_065394.1:n.680+23G>A
NM_020533.3:c.680+23G>A MANE Select NP_065394.1:n.680+23G>A