Canonical Allele Identifier: CA2320965592
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533852A= , CM000681.2:g.7533852A= GRCh38
NC_000019.9:g.7598738A= , CM000681.1:g.7598738A= GRCh37
NC_000019.8:g.7504738A= NCBI36
NG_013374.1:g.4701A=
NG_015806.1:g.16243A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*57A= MANE Select ENSP00000264079.5:n.*57A=
ENST00000264079.10:c.*57A= ENSP00000264079.5:n.*57A=
ENST00000394321.9:n.2115A=
ENST00000599334.1:c.528A=
ENST00000601870.1:c.153A=
ENST00000602227.1:n.354A=
NM_020533.2:c.*57A= NP_065394.1:n.*57A=
NM_020533.3:c.*57A= MANE Select NP_065394.1:n.*57A=