Canonical Allele Identifier: CA2320961784
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526441C= , CM000681.2:g.7526441C= GRCh38
NC_000019.9:g.7591327C= , CM000681.1:g.7591327C= GRCh37
NC_000019.8:g.7497327C= NCBI36
NG_015806.1:g.8832C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.240C= MANE Select ENSP00000264079.5:p.Leu80=
ENST00000264079.10:c.240C= ENSP00000264079.5:p.Leu80=
ENST00000394321.9:n.320C=
ENST00000596008.1:n.202C=
ENST00000598406.1:n.61C=
ENST00000601003.1:c.240C= ENSP00000469074.1:p.Leu80=
NM_020533.2:c.240C= NP_065394.1:p.Leu80=
NM_020533.3:c.240C= MANE Select NP_065394.1:p.Leu80=