Canonical Allele Identifier: CA2320962006
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526860T= , CM000681.2:g.7526860T= GRCh38
NC_000019.9:g.7591746T= , CM000681.1:g.7591746T= GRCh37
NC_000019.8:g.7497746T= NCBI36
NG_015806.1:g.9251T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.505T= MANE Select ENSP00000264079.5:p.Tyr169=
ENST00000264079.10:c.505T= ENSP00000264079.5:p.Tyr169=
ENST00000394321.9:n.585T=
ENST00000596008.1:n.467T=
ENST00000598406.1:n.326T=
ENST00000601003.1:c.505T= ENSP00000469074.1:p.Tyr169=
NM_020533.2:c.505T= NP_065394.1:p.Tyr169=
NM_020533.3:c.505T= MANE Select NP_065394.1:p.Tyr169=