Canonical Allele Identifier: CA1272520781

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250901_96250903delinsAAC , CM000664.2:g.96250901_96250903delinsAAC	GRCh38
NC_000002.11:g.96916639_96916641delinsAAC , CM000664.1:g.96916639_96916641delinsAAC	GRCh37
NC_000002.10:g.96280366_96280368delinsAAC	NCBI36
NG_027695.1:g.20111_20113delinsGTT , LRG_528:g.20111_20113delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2905_*2907delinsGTT MANE Select	ENSP00000258439.3:n.*2905_*2907delinsGTT
ENST00000258439.7:c.*2905_*2907delinsGTT	ENSP00000258439.2:n.*2905_*2907delinsGTT
NM_001193304.2:c.*2905_*2907delinsGTT	NP_001180233.1:n.*2905_*2907delinsGTT
NM_017849.3:c.*2905_*2907delinsGTT , LRG_528t1:c.*2905_*2907delinsGTT	NP_060319.1:n.*2905_*2907delinsGTT
XM_017004450.1:c.*2206_*2208delinsGTT	XP_016859939.1:n.*2206_*2208delinsGTT
XM_017004452.1:c.*2905_*2907delinsGTT	XP_016859941.1:n.*2905_*2907delinsGTT
NM_001193304.3:c.*2905_*2907delinsGTT	NP_001180233.1:n.*2905_*2907delinsGTT
NM_017849.4:c.*2905_*2907delinsGTT MANE Select	NP_060319.1:n.*2905_*2907delinsGTT