Canonical Allele Identifier: CA2660175398
Gene: TMEM127 HGNC NCBI

Linked Data

gnomAD v4: 2-96251537-G-GAA
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251545_96251546dup , CM000664.2:g.96251545_96251546dup GRCh38
NC_000002.11:g.96917283_96917284dup , CM000664.1:g.96917283_96917284dup GRCh37
NC_000002.10:g.96281010_96281011dup NCBI36
NG_027695.1:g.19475_19476dup , LRG_528:g.19475_19476dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2269_*2270dup MANE Select ENSP00000258439.3:n.*2269_*2270dup
ENST00000258439.7:c.*2269_*2270dup ENSP00000258439.2:n.*2269_*2270dup
NM_001193304.2:c.*2269_*2270dup NP_001180233.1:n.*2269_*2270dup
NM_017849.3:c.*2269_*2270dup , LRG_528t1:c.*2269_*2270dup NP_060319.1:n.*2269_*2270dup
XM_017004450.1:c.*1570_*1571dup XP_016859939.1:n.*1570_*1571dup
XM_017004452.1:c.*2269_*2270dup XP_016859941.1:n.*2269_*2270dup
NM_001193304.3:c.*2269_*2270dup NP_001180233.1:n.*2269_*2270dup
NM_017849.4:c.*2269_*2270dup MANE Select NP_060319.1:n.*2269_*2270dup
Search 100 bp 5'
Search 100 bp 3'