Canonical Allele Identifier: CA2320961179
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525016A= , CM000681.2:g.7525016A= GRCh38
NC_000019.9:g.7589902A= , CM000681.1:g.7589902A= GRCh37
NC_000019.8:g.7495902A= NCBI36
NG_015806.1:g.7407A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.87A= MANE Select ENSP00000264079.5:p.Ser29=
ENST00000264079.10:c.87A= ENSP00000264079.5:p.Ser29=
ENST00000394321.9:n.167A=
ENST00000596390.1:n.203A=
ENST00000601003.1:c.87A= ENSP00000469074.1:p.Ser29=
NM_020533.2:c.87A= NP_065394.1:p.Ser29=
NM_020533.3:c.87A= MANE Select NP_065394.1:p.Ser29=