Canonical Allele Identifier: CA2320965572
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533835A= , CM000681.2:g.7533835A= GRCh38
NC_000019.9:g.7598721A= , CM000681.1:g.7598721A= GRCh37
NC_000019.8:g.7504721A= NCBI36
NG_013374.1:g.4684A=
NG_015806.1:g.16226A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*40A= MANE Select ENSP00000264079.5:n.*40A=
ENST00000264079.10:c.*40A= ENSP00000264079.5:n.*40A=
ENST00000394321.9:n.2098A=
ENST00000599334.1:c.511A=
ENST00000601870.1:c.136A=
ENST00000602227.1:n.337A=
NM_020533.2:c.*40A= NP_065394.1:n.*40A=
NM_020533.3:c.*40A= MANE Select NP_065394.1:n.*40A=