Canonical Allele Identifier: CA2320965495
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533665G= , CM000681.2:g.7533665G= GRCh38
NC_000019.9:g.7598551G= , CM000681.1:g.7598551G= GRCh37
NC_000019.8:g.7504551G= NCBI36
NG_013374.1:g.4514G=
NG_015806.1:g.16056G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1706+12G= MANE Select ENSP00000264079.5:n.1706+12G=
ENST00000264079.10:c.1706+12G= ENSP00000264079.5:n.1706+12G=
ENST00000394321.9:n.2021+12G=
ENST00000599334.1:c.434+12G=
ENST00000601870.1:c.59+12G=
ENST00000602227.1:n.260+12G=
NM_020533.2:c.1706+12G= NP_065394.1:n.1706+12G=
NM_020533.3:c.1706+12G= MANE Select NP_065394.1:n.1706+12G=