Canonical Allele Identifier: CA646526657
Gene: TMEM127 HGNC NCBI

Linked Data

COSMIC: COSN14843238
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251764_96251765insT , CM000664.2:g.96251764_96251765insT GRCh38
NC_000002.11:g.96917502_96917503insT , CM000664.1:g.96917502_96917503insT GRCh37
NC_000002.10:g.96281229_96281230insT NCBI36
NG_027695.1:g.19249_19250insA , LRG_528:g.19249_19250insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2043_*2044insA MANE Select ENSP00000258439.3:n.*2043_*2044insA
ENST00000258439.7:c.*2043_*2044insA ENSP00000258439.2:n.*2043_*2044insA
ENST00000432959.1:c.*2043_*2044insA ENSP00000416660.1:n.*2043_*2044insA
NM_001193304.2:c.*2043_*2044insA NP_001180233.1:n.*2043_*2044insA
NM_017849.3:c.*2043_*2044insA , LRG_528t1:c.*2043_*2044insA NP_060319.1:n.*2043_*2044insA
XM_017004450.1:c.*1344_*1345insA XP_016859939.1:n.*1344_*1345insA
XM_017004452.1:c.*2043_*2044insA XP_016859941.1:n.*2043_*2044insA
NM_001193304.3:c.*2043_*2044insA NP_001180233.1:n.*2043_*2044insA
NM_017849.4:c.*2043_*2044insA MANE Select NP_060319.1:n.*2043_*2044insA
Search 100 bp 5'
Search 100 bp 3'