Canonical Allele Identifier: CA505226283
Gene: MCOLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1078293
ClinVar RCV Id: RCV001393209
dbSNP Id: rs2022568652
gnomAD v3: 19-7526450-T-C
gnomAD v4: 19-7526450-T-C
MyVariant Identifiers: chr19:g.7591336T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526450T>C , CM000681.2:g.7526450T>C GRCh38
NC_000019.9:g.7591336T>C , CM000681.1:g.7591336T>C GRCh37
NC_000019.8:g.7497336T>C NCBI36
NG_015806.1:g.8841T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.249T>C MANE Select ENSP00000264079.5:p.Phe83=
ENST00000264079.10:c.249T>C ENSP00000264079.5:p.Phe83=
ENST00000394321.9:n.329T>C
ENST00000596008.1:n.211T>C
ENST00000598406.1:n.70T>C
ENST00000601003.1:c.249T>C ENSP00000469074.1:p.Phe83=
NM_020533.2:c.249T>C NP_065394.1:p.Phe83=
NM_020533.3:c.249T>C MANE Select NP_065394.1:p.Phe83=