Canonical Allele Identifier: CA2320962939
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528709G= , CM000681.2:g.7528709G= GRCh38
NC_000019.9:g.7593595G= , CM000681.1:g.7593595G= GRCh37
NC_000019.8:g.7499595G= NCBI36
NG_015806.1:g.11100G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.984+6G= MANE Select ENSP00000264079.5:n.984+6G=
ENST00000264079.10:c.984+6G= ENSP00000264079.5:n.984+6G=
ENST00000394321.9:n.1299+6G=
ENST00000595860.5:n.56G=
NM_020533.2:c.984+6G= NP_065394.1:n.984+6G=
NM_020533.3:c.984+6G= MANE Select NP_065394.1:n.984+6G=