Canonical Allele Identifier: CA2320965610
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533885A= , CM000681.2:g.7533885A= GRCh38
NC_000019.9:g.7598771A= , CM000681.1:g.7598771A= GRCh37
NC_000019.8:g.7504771A= NCBI36
NG_013374.1:g.4734A=
NG_015806.1:g.16276A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*90A= MANE Select ENSP00000264079.5:n.*90A=
ENST00000264079.10:c.*90A= ENSP00000264079.5:n.*90A=
ENST00000394321.9:n.2148A=
ENST00000599334.1:c.561A=
ENST00000601870.1:c.169+17A=
ENST00000602227.1:n.387A=
NM_020533.2:c.*90A= NP_065394.1:n.*90A=
NM_020533.3:c.*90A= MANE Select NP_065394.1:n.*90A=