Canonical Allele Identifier: CA2320962695
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528210C= , CM000681.2:g.7528210C= GRCh38
NC_000019.9:g.7593096C= , CM000681.1:g.7593096C= GRCh37
NC_000019.8:g.7499096C= NCBI36
NG_015806.1:g.10601C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.830C= MANE Select ENSP00000264079.5:p.Thr277=
ENST00000264079.10:c.830C= ENSP00000264079.5:p.Thr277=
ENST00000394321.9:n.1145C=
NM_020533.2:c.830C= NP_065394.1:p.Thr277=
NM_020533.3:c.830C= MANE Select NP_065394.1:p.Thr277=
Search 100 bp 5'
Search 100 bp 3'