Canonical Allele Identifier: CA2320963755
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530248T= , CM000681.2:g.7530248T= GRCh38
NC_000019.9:g.7595134T= , CM000681.1:g.7595134T= GRCh37
NC_000019.8:g.7501134T= NCBI36
NG_013374.1:g.1097T=
NG_015806.1:g.12639T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1360-38T= MANE Select ENSP00000264079.5:n.1360-38T=
ENST00000264079.10:c.1360-38T= ENSP00000264079.5:n.1360-38T=
ENST00000394321.9:n.1675-38T=
ENST00000594692.1:n.356-38T=
ENST00000595860.5:n.543-38T=
ENST00000599334.1:c.237-187T=
NM_020533.2:c.1360-38T= NP_065394.1:n.1360-38T=
NM_020533.3:c.1360-38T= MANE Select NP_065394.1:n.1360-38T=