Canonical Allele Identifier: CA2320965614
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533894T= , CM000681.2:g.7533894T= GRCh38
NC_000019.9:g.7598780T= , CM000681.1:g.7598780T= GRCh37
NC_000019.8:g.7504780T= NCBI36
NG_013374.1:g.4743T=
NG_015806.1:g.16285T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*99T= MANE Select ENSP00000264079.5:n.*99T=
ENST00000264079.10:c.*99T= ENSP00000264079.5:n.*99T=
ENST00000394321.9:n.2157T=
ENST00000599334.1:c.570T=
ENST00000601870.1:c.169+26T=
ENST00000602227.1:n.396T=
NM_020533.2:c.*99T= NP_065394.1:n.*99T=
NM_020533.3:c.*99T= MANE Select NP_065394.1:n.*99T=