Canonical Allele Identifier: CA2320965573
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533839A= , CM000681.2:g.7533839A= GRCh38
NC_000019.9:g.7598725A= , CM000681.1:g.7598725A= GRCh37
NC_000019.8:g.7504725A= NCBI36
NG_013374.1:g.4688A=
NG_015806.1:g.16230A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*44A= MANE Select ENSP00000264079.5:n.*44A=
ENST00000264079.10:c.*44A= ENSP00000264079.5:n.*44A=
ENST00000394321.9:n.2102A=
ENST00000599334.1:c.515A=
ENST00000601870.1:c.140A=
ENST00000602227.1:n.341A=
NM_020533.2:c.*44A= NP_065394.1:n.*44A=
NM_020533.3:c.*44A= MANE Select NP_065394.1:n.*44A=