Canonical Allele Identifier: CA2320962350
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527532T= , CM000681.2:g.7527532T= GRCh38
NC_000019.9:g.7592418T= , CM000681.1:g.7592418T= GRCh37
NC_000019.8:g.7498418T= NCBI36
NG_015806.1:g.9923T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.584T= MANE Select ENSP00000264079.5:p.Val195=
ENST00000264079.10:c.584T= ENSP00000264079.5:p.Val195=
ENST00000394321.9:n.664T=
ENST00000598406.1:n.405T=
ENST00000601003.1:c.572-332T= ENSP00000469074.1:n.572-332T=
NM_020533.2:c.584T= NP_065394.1:p.Val195=
NM_020533.3:c.584T= MANE Select NP_065394.1:p.Val195=