Canonical Allele Identifier: CA347655998
Gene: TMEM127 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265222A>T , CM000664.2:g.96265222A>T GRCh38
NC_000002.11:g.96930960A>T , CM000664.1:g.96930960A>T GRCh37
NC_000002.10:g.96294687A>T NCBI36
NG_027695.1:g.5792T>A , LRG_528:g.5792T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.160T>A MANE Select ENSP00000258439.3:p.Leu54Met
ENST00000258439.7:c.160T>A ENSP00000258439.2:p.Leu54Met
ENST00000432959.1:c.160T>A ENSP00000416660.1:p.Leu54Met
NM_001193304.2:c.160T>A NP_001180233.1:p.Leu54Met
NM_017849.3:c.160T>A , LRG_528t1:c.160T>A NP_060319.1:p.Leu54Met
NM_001193304.3:c.160T>A NP_001180233.1:p.Leu54Met
NM_017849.4:c.160T>A MANE Select NP_060319.1:p.Leu54Met