Canonical Allele Identifier: CA1272522090
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96253970_96253983delinsTCCACCAGCTCCTG , CM000664.2:g.96253970_96253983delinsTCCACCAGCTCCTG GRCh38
NC_000002.11:g.96919708_96919721delinsTCCACCAGCTCCTG , CM000664.1:g.96919708_96919721delinsTCCACCAGCTCCTG GRCh37
NC_000002.10:g.96283435_96283448delinsTCCACCAGCTCCTG NCBI36
NG_027695.1:g.17031_17044delinsCAGGAGCTGGTGGA , LRG_528:g.17031_17044delinsCAGGAGCTGGTGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.542_555delinsCAGGAGCTGGTGGA MANE Select ENSP00000258439.3:p.Ala181=
ENST00000258439.7:c.542_555delinsCAGGAGCTGGTGGA ENSP00000258439.2:p.Ala181=
ENST00000432959.1:c.542_555delinsCAGGAGCTGGTGGA ENSP00000416660.1:p.Ala181=
ENST00000435268.1:c.290_303delinsCAGGAGCTGGTGGA ENSP00000411810.1:p.Ala97=
NM_001193304.2:c.542_555delinsCAGGAGCTGGTGGA NP_001180233.1:p.Ala181=
NM_017849.3:c.542_555delinsCAGGAGCTGGTGGA , LRG_528t1:c.542_555delinsCAGGAGCTGGTGGA NP_060319.1:p.Ala181=
XM_017004450.1:c.-377_-364delinsCAGGAGCTGGTGGA XP_016859939.1:n.-377_-364delinsCAGGAGCTG...
XM_017004452.1:c.290_303delinsCAGGAGCTGGTGGA XP_016859941.1:p.Ala97=
NM_001193304.3:c.542_555delinsCAGGAGCTGGTGGA NP_001180233.1:p.Ala181=
NM_017849.4:c.542_555delinsCAGGAGCTGGTGGA MANE Select NP_060319.1:p.Ala181=