Canonical Allele Identifier: CA2320962750
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528321G= , CM000681.2:g.7528321G= GRCh38
NC_000019.9:g.7593207G= , CM000681.1:g.7593207G= GRCh37
NC_000019.8:g.7499207G= NCBI36
NG_015806.1:g.10712G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.877+64G= MANE Select ENSP00000264079.5:n.877+64G=
ENST00000264079.10:c.877+64G= ENSP00000264079.5:n.877+64G=
ENST00000394321.9:n.1192+64G=
NM_020533.2:c.877+64G= NP_065394.1:n.877+64G=
NM_020533.3:c.877+64G= MANE Select NP_065394.1:n.877+64G=