Canonical Allele Identifier: CA2320963036
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528907G= , CM000681.2:g.7528907G= GRCh38
NC_000019.9:g.7593793G= , CM000681.1:g.7593793G= GRCh37
NC_000019.8:g.7499793G= NCBI36
NG_015806.1:g.11298G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1071G= MANE Select ENSP00000264079.5:p.Leu357=
ENST00000264079.10:c.1071G= ENSP00000264079.5:p.Leu357=
ENST00000394321.9:n.1386G=
ENST00000595860.5:n.254G=
NM_020533.2:c.1071G= NP_065394.1:p.Leu357=
NM_020533.3:c.1071G= MANE Select NP_065394.1:p.Leu357=