Canonical Allele Identifier: CA1272521068
Gene: TMEM127 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251525_96251528delinsAAAC , CM000664.2:g.96251525_96251528delinsAAAC GRCh38
NC_000002.11:g.96917263_96917266delinsAAAC , CM000664.1:g.96917263_96917266delinsAAAC GRCh37
NC_000002.10:g.96280990_96280993delinsAAAC NCBI36
NG_027695.1:g.19486_19489delinsGTTT , LRG_528:g.19486_19489delinsGTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*2280_*2283delinsGTTT MANE Select ENSP00000258439.3:n.*2280_*2283delinsGTTT
ENST00000258439.7:c.*2280_*2283delinsGTTT ENSP00000258439.2:n.*2280_*2283delinsGTTT
NM_001193304.2:c.*2280_*2283delinsGTTT NP_001180233.1:n.*2280_*2283delinsGTTT
NM_017849.3:c.*2280_*2283delinsGTTT , LRG_528t1:c.*2280_*2283delinsGTTT NP_060319.1:n.*2280_*2283delinsGTTT
XM_017004450.1:c.*1581_*1584delinsGTTT XP_016859939.1:n.*1581_*1584delinsGTTT
XM_017004452.1:c.*2280_*2283delinsGTTT XP_016859941.1:n.*2280_*2283delinsGTTT
NM_001193304.3:c.*2280_*2283delinsGTTT NP_001180233.1:n.*2280_*2283delinsGTTT
NM_017849.4:c.*2280_*2283delinsGTTT MANE Select NP_060319.1:n.*2280_*2283delinsGTTT
Search 100 bp 5'
Search 100 bp 3'