Canonical Allele Identifier: CA403081393
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526828C>A , CM000681.2:g.7526828C>A GRCh38
NC_000019.9:g.7591714C>A , CM000681.1:g.7591714C>A GRCh37
NC_000019.8:g.7497714C>A NCBI36
NG_015806.1:g.9219C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.473C>A MANE Select ENSP00000264079.5:p.Thr158Asn
ENST00000264079.10:c.473C>A ENSP00000264079.5:p.Thr158Asn
ENST00000394321.9:n.553C>A
ENST00000596008.1:n.435C>A
ENST00000598406.1:n.294C>A
ENST00000601003.1:c.473C>A ENSP00000469074.1:p.Thr158Asn
NM_020533.2:c.473C>A NP_065394.1:p.Thr158Asn
NM_020533.3:c.473C>A MANE Select NP_065394.1:p.Thr158Asn