Canonical Allele Identifier: CA2320965596
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533856C= , CM000681.2:g.7533856C= GRCh38
NC_000019.9:g.7598742C= , CM000681.1:g.7598742C= GRCh37
NC_000019.8:g.7504742C= NCBI36
NG_013374.1:g.4705C=
NG_015806.1:g.16247C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*61C= MANE Select ENSP00000264079.5:n.*61C=
ENST00000264079.10:c.*61C= ENSP00000264079.5:n.*61C=
ENST00000394321.9:n.2119C=
ENST00000599334.1:c.532C=
ENST00000601870.1:c.157C=
ENST00000602227.1:n.358C=
NM_020533.2:c.*61C= NP_065394.1:n.*61C=
NM_020533.3:c.*61C= MANE Select NP_065394.1:n.*61C=