Canonical Allele Identifier: CA2320962480
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1568399149
gnomAD v4: 19-7527743-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527743G>T , CM000681.2:g.7527743G>T GRCh38
NC_000019.9:g.7592629G>T , CM000681.1:g.7592629G>T GRCh37
NC_000019.8:g.7498629G>T NCBI36
NG_015806.1:g.10134G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.680+115G>T MANE Select ENSP00000264079.5:n.680+115G>T
ENST00000264079.10:c.680+115G>T ENSP00000264079.5:n.680+115G>T
ENST00000394321.9:n.875G>T
ENST00000598406.1:n.616G>T
ENST00000601003.1:c.572-121G>T ENSP00000469074.1:n.572-121G>T
NM_020533.2:c.680+115G>T NP_065394.1:n.680+115G>T
NM_020533.3:c.680+115G>T MANE Select NP_065394.1:n.680+115G>T