Canonical Allele Identifier: CA2751311961

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96253990_96254064del , CM000664.2:g.96253990_96254064del	GRCh38
NC_000002.11:g.96919728_96919802del , CM000664.1:g.96919728_96919802del	GRCh37
NC_000002.10:g.96283455_96283529del	NCBI36
NG_027695.1:g.16951_17025del , LRG_528:g.16951_17025del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.462_536del MANE Select	ENSP00000258439.3:p.Ile154_Leu179delinsMet
ENST00000258439.7:c.462_536del	ENSP00000258439.2:p.Ile154_Leu179delinsMet
ENST00000432959.1:c.462_536del	ENSP00000416660.1:p.Ile154_Leu179delinsMet
ENST00000435268.1:c.210_284del	ENSP00000411810.1:p.Ile70_Leu95delinsMet
NM_001193304.2:c.462_536del	NP_001180233.1:p.Ile154_Leu179delinsMet
NM_017849.3:c.462_536del , LRG_528t1:c.462_536del	NP_060319.1:p.Ile154_Leu179delinsMet
XM_017004450.1:c.-457_-383del	XP_016859939.1:n.-457_-383del
XM_017004452.1:c.210_284del	XP_016859941.1:p.Ile70_Leu95delinsMet
NM_001193304.3:c.462_536del	NP_001180233.1:p.Ile154_Leu179delinsMet
NM_017849.4:c.462_536del MANE Select	NP_060319.1:p.Ile154_Leu179delinsMet