Canonical Allele Identifier: CA2660175211
Gene: TMEM127 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251360del , CM000664.2:g.96251360del GRCh38
NC_000002.11:g.96917098del , CM000664.1:g.96917098del GRCh37
NC_000002.10:g.96280825del NCBI36
NG_027695.1:g.19658del , LRG_528:g.19658del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2452del MANE Select ENSP00000258439.3:n.*2452del
ENST00000258439.7:c.*2452del ENSP00000258439.2:n.*2452del
NM_001193304.2:c.*2452del NP_001180233.1:n.*2452del
NM_017849.3:c.*2452del , LRG_528t1:c.*2452del NP_060319.1:n.*2452del
XM_017004450.1:c.*1753del XP_016859939.1:n.*1753del
XM_017004452.1:c.*2452del XP_016859941.1:n.*2452del
NM_001193304.3:c.*2452del NP_001180233.1:n.*2452del
NM_017849.4:c.*2452del MANE Select NP_060319.1:n.*2452del