Canonical Allele Identifier: CA2320965669
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533994G= , CM000681.2:g.7533994G= GRCh38
NC_000019.9:g.7598880G= , CM000681.1:g.7598880G= GRCh37
NC_000019.8:g.7504880G= NCBI36
NG_013374.1:g.4843G=
NG_015806.1:g.16385G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*199G= MANE Select ENSP00000264079.5:n.*199G=
ENST00000264079.10:c.*199G= ENSP00000264079.5:n.*199G=
ENST00000601870.1:c.169+126G=
NM_020533.2:c.*199G= NP_065394.1:n.*199G=
NM_020533.3:c.*199G= MANE Select NP_065394.1:n.*199G=