Canonical Allele Identifier: CA2320961808
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526502_7526504delinsTTC , CM000681.2:g.7526502_7526504delinsTTC GRCh38
NC_000019.9:g.7591388_7591390delinsTTC , CM000681.1:g.7591388_7591390delinsTTC GRCh37
NC_000019.8:g.7497388_7497390delinsTTC NCBI36
NG_015806.1:g.8893_8895delinsTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.301_303delinsTTC MANE Select ENSP00000264079.5:p.Phe101=
ENST00000264079.10:c.301_303delinsTTC ENSP00000264079.5:p.Phe101=
ENST00000394321.9:n.381_383delinsTTC
ENST00000596008.1:n.263_265delinsTTC
ENST00000598406.1:n.122_124delinsTTC
ENST00000601003.1:c.301_303delinsTTC ENSP00000469074.1:p.Phe101=
NM_020533.2:c.301_303delinsTTC NP_065394.1:p.Phe101=
NM_020533.3:c.301_303delinsTTC MANE Select NP_065394.1:p.Phe101=