Canonical Allele Identifier: CA2320965579
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533842C= , CM000681.2:g.7533842C= GRCh38
NC_000019.9:g.7598728C= , CM000681.1:g.7598728C= GRCh37
NC_000019.8:g.7504728C= NCBI36
NG_013374.1:g.4691C=
NG_015806.1:g.16233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*47C= MANE Select ENSP00000264079.5:n.*47C=
ENST00000264079.10:c.*47C= ENSP00000264079.5:n.*47C=
ENST00000394321.9:n.2105C=
ENST00000599334.1:c.518C=
ENST00000601870.1:c.143C=
ENST00000602227.1:n.344C=
NM_020533.2:c.*47C= NP_065394.1:n.*47C=
NM_020533.3:c.*47C= MANE Select NP_065394.1:n.*47C=