Canonical Allele Identifier: CA1272521175
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251759_96251767delinsCAGAGGGAA , CM000664.2:g.96251759_96251767delinsCAGAGGGAA GRCh38
NC_000002.11:g.96917497_96917505delinsCAGAGGGAA , CM000664.1:g.96917497_96917505delinsCAGAGGGAA GRCh37
NC_000002.10:g.96281224_96281232delinsCAGAGGGAA NCBI36
NG_027695.1:g.19247_19255delinsTTCCCTCTG , LRG_528:g.19247_19255delinsTTCCCTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2041_*2049delinsTTCCCTCTG MANE Select ENSP00000258439.3:n.*2041_*2049delinsTTCCCTCTG
ENST00000258439.7:c.*2041_*2049delinsTTCCCTCTG ENSP00000258439.2:n.*2041_*2049delinsTTCCCTCTG
ENST00000432959.1:c.*2041_*2049delinsTTCCCTCTG ENSP00000416660.1:n.*2041_*2049delinsTTCCCTCTG
NM_001193304.2:c.*2041_*2049delinsTTCCCTCTG NP_001180233.1:n.*2041_*2049delinsTTCCCTCTG
NM_017849.3:c.*2041_*2049delinsTTCCCTCTG , LRG_528t1:c.*2041_*2049delinsTTCCCTCTG NP_060319.1:n.*2041_*2049delinsTTCCCTCTG
XM_017004450.1:c.*1342_*1350delinsTTCCCTCTG XP_016859939.1:n.*1342_*1350delinsTTCCCTCTG
XM_017004452.1:c.*2041_*2049delinsTTCCCTCTG XP_016859941.1:n.*2041_*2049delinsTTCCCTCTG
NM_001193304.3:c.*2041_*2049delinsTTCCCTCTG NP_001180233.1:n.*2041_*2049delinsTTCCCTCTG
NM_017849.4:c.*2041_*2049delinsTTCCCTCTG MANE Select NP_060319.1:n.*2041_*2049delinsTTCCCTCTG