Canonical Allele Identifier: CA505226699
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1264915460
gnomAD v2: 19-7591399-C-G
gnomAD v4: 19-7526513-C-G

Genomic Alleles

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

Transcript Alleles

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