Canonical Allele Identifier: CA2660174979
Gene: TMEM127 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251052del , CM000664.2:g.96251052del GRCh38
NC_000002.11:g.96916790del , CM000664.1:g.96916790del GRCh37
NC_000002.10:g.96280517del NCBI36
NG_027695.1:g.19962del , LRG_528:g.19962del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2756del MANE Select ENSP00000258439.3:n.*2756del
ENST00000258439.7:c.*2756del ENSP00000258439.2:n.*2756del
NM_001193304.2:c.*2756del NP_001180233.1:n.*2756del
NM_017849.3:c.*2756del , LRG_528t1:c.*2756del NP_060319.1:n.*2756del
XM_017004450.1:c.*2057del XP_016859939.1:n.*2057del
XM_017004452.1:c.*2756del XP_016859941.1:n.*2756del
NM_001193304.3:c.*2756del NP_001180233.1:n.*2756del
NM_017849.4:c.*2756del MANE Select NP_060319.1:n.*2756del