Canonical Allele Identifier: CA2320963698
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530138C= , CM000681.2:g.7530138C= GRCh38
NC_000019.9:g.7595024C= , CM000681.1:g.7595024C= GRCh37
NC_000019.8:g.7501024C= NCBI36
NG_013374.1:g.987C=
NG_015806.1:g.12529C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1360-148C= MANE Select ENSP00000264079.5:n.1360-148C=
ENST00000264079.10:c.1360-148C= ENSP00000264079.5:n.1360-148C=
ENST00000394321.9:n.1675-148C=
ENST00000594692.1:n.356-148C=
ENST00000595860.5:n.543-148C=
ENST00000599334.1:c.237-297C=
NM_020533.2:c.1360-148C= NP_065394.1:n.1360-148C=
NM_020533.3:c.1360-148C= MANE Select NP_065394.1:n.1360-148C=