Canonical Allele Identifier: CA2320963077
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528999G= , CM000681.2:g.7528999G= GRCh38
NC_000019.9:g.7593885G= , CM000681.1:g.7593885G= GRCh37
NC_000019.8:g.7499885G= NCBI36
NG_015806.1:g.11390G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1134+29G= MANE Select ENSP00000264079.5:n.1134+29G=
ENST00000264079.10:c.1134+29G= ENSP00000264079.5:n.1134+29G=
ENST00000394321.9:n.1449+29G=
ENST00000594692.1:n.29G=
ENST00000595860.5:n.317+29G=
ENST00000599334.1:c.11+29G=
NM_020533.2:c.1134+29G= NP_065394.1:n.1134+29G=
NM_020533.3:c.1134+29G= MANE Select NP_065394.1:n.1134+29G=
Search 100 bp 5'
Search 100 bp 3'