Canonical Allele Identifier: CA1272521464

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96252408_96252409delinsAG , CM000664.2:g.96252408_96252409delinsAG	GRCh38
NC_000002.11:g.96918146_96918147delinsAG , CM000664.1:g.96918146_96918147delinsAG	GRCh37
NC_000002.10:g.96281873_96281874delinsAG	NCBI36
NG_027695.1:g.18605_18606delinsCT , LRG_528:g.18605_18606delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*1399_*1400delinsCT MANE Select	ENSP00000258439.3:n.*1399_*1400delinsCT
ENST00000258439.7:c.*1399_*1400delinsCT	ENSP00000258439.2:n.*1399_*1400delinsCT
ENST00000432959.1:c.*1399_*1400delinsCT	ENSP00000416660.1:n.*1399_*1400delinsCT
NM_001193304.2:c.*1399_*1400delinsCT	NP_001180233.1:n.*1399_*1400delinsCT
NM_017849.3:c.*1399_*1400delinsCT , LRG_528t1:c.*1399_*1400delinsCT	NP_060319.1:n.*1399_*1400delinsCT
XM_017004450.1:c.*700_*701delinsCT	XP_016859939.1:n.*700_*701delinsCT
XM_017004452.1:c.*1399_*1400delinsCT	XP_016859941.1:n.*1399_*1400delinsCT
NM_001193304.3:c.*1399_*1400delinsCT	NP_001180233.1:n.*1399_*1400delinsCT
NM_017849.4:c.*1399_*1400delinsCT MANE Select	NP_060319.1:n.*1399_*1400delinsCT