Canonical Allele Identifier: CA1272522188

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254159_96254160delinsTC , CM000664.2:g.96254159_96254160delinsTC	GRCh38
NC_000002.11:g.96919897_96919898delinsTC , CM000664.1:g.96919897_96919898delinsTC	GRCh37
NC_000002.10:g.96283624_96283625delinsTC	NCBI36
NG_027695.1:g.16854_16855delinsGA , LRG_528:g.16854_16855delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.410-45_410-44delinsGA MANE Select	ENSP00000258439.3:n.410-45_410-44delinsGA
ENST00000258439.7:c.410-45_410-44delinsGA	ENSP00000258439.2:n.410-45_410-44delinsGA
ENST00000432959.1:c.410-45_410-44delinsGA	ENSP00000416660.1:n.410-45_410-44delinsGA
ENST00000435268.1:c.158-45_158-44delinsGA	ENSP00000411810.1:n.158-45_158-44delinsGA
NM_001193304.2:c.410-45_410-44delinsGA	NP_001180233.1:n.410-45_410-44delinsGA
NM_017849.3:c.410-45_410-44delinsGA , LRG_528t1:c.410-45_410-44delinsGA	NP_060319.1:n.410-45_410-44delinsGA
XM_017004450.1:c.-509-45_-509-44delinsGA	XP_016859939.1:n.-509-45_-509-44delinsGA
XM_017004452.1:c.158-45_158-44delinsGA	XP_016859941.1:n.158-45_158-44delinsGA
NM_001193304.3:c.410-45_410-44delinsGA	NP_001180233.1:n.410-45_410-44delinsGA
NM_017849.4:c.410-45_410-44delinsGA MANE Select	NP_060319.1:n.410-45_410-44delinsGA