Canonical Allele Identifier: CA403152372
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7524985A>G , CM000681.2:g.7524985A>G GRCh38
NC_000019.9:g.7589871A>G , CM000681.1:g.7589871A>G GRCh37
NC_000019.8:g.7495871A>G NCBI36
NG_015806.1:g.7376A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.56A>G MANE Select ENSP00000264079.5:p.Asn19Ser
ENST00000264079.10:c.56A>G ENSP00000264079.5:p.Asn19Ser
ENST00000394321.9:n.136A>G
ENST00000596390.1:n.172A>G
ENST00000601003.1:c.56A>G ENSP00000469074.1:p.Asn19Ser
NM_020533.2:c.56A>G NP_065394.1:p.Asn19Ser
NM_020533.3:c.56A>G MANE Select NP_065394.1:p.Asn19Ser