Canonical Allele Identifier: CA2660174818
Gene: TMEM127 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96250589_96250608del , CM000664.2:g.96250589_96250608del GRCh38
NC_000002.11:g.96916327_96916346del , CM000664.1:g.96916327_96916346del GRCh37
NC_000002.10:g.96280054_96280073del NCBI36
NG_027695.1:g.20406_20425del , LRG_528:g.20406_20425del

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*3200_*3219del MANE Select ENSP00000258439.3:n.*3200_*3219del
ENST00000258439.7:c.*3200_*3219del ENSP00000258439.2:n.*3200_*3219del
NM_001193304.2:c.*3200_*3219del NP_001180233.1:n.*3200_*3219del
NM_017849.3:c.*3200_*3219del , LRG_528t1:c.*3200_*3219del NP_060319.1:n.*3200_*3219del
XM_017004450.1:c.*2501_*2520del XP_016859939.1:n.*2501_*2520del
XM_017004452.1:c.*3200_*3219del XP_016859941.1:n.*3200_*3219del
NM_001193304.3:c.*3200_*3219del NP_001180233.1:n.*3200_*3219del
NM_017849.4:c.*3200_*3219del MANE Select NP_060319.1:n.*3200_*3219del