Canonical Allele Identifier: CA2320963037
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528910C= , CM000681.2:g.7528910C= GRCh38
NC_000019.9:g.7593796C= , CM000681.1:g.7593796C= GRCh37
NC_000019.8:g.7499796C= NCBI36
NG_015806.1:g.11301C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1074C= MANE Select ENSP00000264079.5:p.Leu358=
ENST00000264079.10:c.1074C= ENSP00000264079.5:p.Leu358=
ENST00000394321.9:n.1389C=
ENST00000595860.5:n.257C=
NM_020533.2:c.1074C= NP_065394.1:p.Leu358=
NM_020533.3:c.1074C= MANE Select NP_065394.1:p.Leu358=