Canonical Allele Identifier: CA2602344457
Gene: TMEM127 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251965dup , CM000664.2:g.96251965dup GRCh38
NC_000002.11:g.96917703dup , CM000664.1:g.96917703dup GRCh37
NC_000002.10:g.96281430dup NCBI36
NG_027695.1:g.19050dup , LRG_528:g.19050dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*1844dup MANE Select ENSP00000258439.3:n.*1844dup
ENST00000258439.7:c.*1844dup ENSP00000258439.2:n.*1844dup
ENST00000432959.1:c.*1844dup ENSP00000416660.1:n.*1844dup
NM_001193304.2:c.*1844dup NP_001180233.1:n.*1844dup
NM_017849.3:c.*1844dup , LRG_528t1:c.*1844dup NP_060319.1:n.*1844dup
XM_017004450.1:c.*1145dup XP_016859939.1:n.*1145dup
XM_017004452.1:c.*1844dup XP_016859941.1:n.*1844dup
NM_001193304.3:c.*1844dup NP_001180233.1:n.*1844dup
NM_017849.4:c.*1844dup MANE Select NP_060319.1:n.*1844dup