Canonical Allele Identifier: CA2320965324
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533585C= , CM000681.2:g.7533585C= GRCh38
NC_000019.9:g.7598471C= , CM000681.1:g.7598471C= GRCh37
NC_000019.8:g.7504471C= NCBI36
NG_013374.1:g.4434C=
NG_015806.1:g.15976C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1638C= MANE Select ENSP00000264079.5:p.Asp546=
ENST00000264079.10:c.1638C= ENSP00000264079.5:p.Asp546=
ENST00000394321.9:n.1953C=
ENST00000599334.1:c.366C=
ENST00000602227.1:n.192C=
NM_020533.2:c.1638C= NP_065394.1:p.Asp546=
NM_020533.3:c.1638C= MANE Select NP_065394.1:p.Asp546=