Canonical Allele Identifier: CA505226696
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1264915460
MyVariant Identifiers: chr19:g.7591399C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526513C>A , CM000681.2:g.7526513C>A GRCh38
NC_000019.9:g.7591399C>A , CM000681.1:g.7591399C>A GRCh37
NC_000019.8:g.7497399C>A NCBI36
NG_015806.1:g.8904C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.312C>A MANE Select ENSP00000264079.5:p.Leu104=
ENST00000264079.10:c.312C>A ENSP00000264079.5:p.Leu104=
ENST00000394321.9:n.392C>A
ENST00000596008.1:n.274C>A
ENST00000598406.1:n.133C>A
ENST00000601003.1:c.312C>A ENSP00000469074.1:p.Leu104=
NM_020533.2:c.312C>A NP_065394.1:p.Leu104=
NM_020533.3:c.312C>A MANE Select NP_065394.1:p.Leu104=