Canonical Allele Identifier: CA2320963536
Gene: MCOLN1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529899A= , CM000681.2:g.7529899A= GRCh38
NC_000019.9:g.7594785A= , CM000681.1:g.7594785A= GRCh37
NC_000019.8:g.7500785A= NCBI36
NG_013374.1:g.748A=
NG_015806.1:g.12290A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1359+187A= MANE Select ENSP00000264079.5:n.1359+187A=
ENST00000264079.10:c.1359+187A= ENSP00000264079.5:n.1359+187A=
ENST00000394321.9:n.1674+187A=
ENST00000594692.1:n.355+187A=
ENST00000595860.5:n.542+187A=
ENST00000599334.1:c.236+187A=
NM_020533.2:c.1359+187A= NP_065394.1:n.1359+187A=
NM_020533.3:c.1359+187A= MANE Select NP_065394.1:n.1359+187A=
Search 100 bp 5'
Search 100 bp 3'