Canonical Allele Identifier: CA2660176937
Gene: TMEM127 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265281del , CM000664.2:g.96265281del GRCh38
NC_000002.11:g.96931019del , CM000664.1:g.96931019del GRCh37
NC_000002.10:g.96294746del NCBI36
NG_027695.1:g.5735del , LRG_528:g.5735del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.103del MANE Select ENSP00000258439.3:p.Leu35CysfsTer?
ENST00000258439.7:c.103del ENSP00000258439.2:p.Leu35CysfsTer?
ENST00000432959.1:c.103del ENSP00000416660.1:p.Leu35CysfsTer?
NM_001193304.2:c.103del NP_001180233.1:p.Leu35CysfsTer?
NM_017849.3:c.103del , LRG_528t1:c.103del NP_060319.1:p.Leu35CysfsTer?
NM_001193304.3:c.103del NP_001180233.1:p.Leu35CysfsTer?
NM_017849.4:c.103del MANE Select NP_060319.1:p.Leu35CysfsTer?