Canonical Allele Identifier: CA1272522041

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96253884_96253886delinsATC , CM000664.2:g.96253884_96253886delinsATC	GRCh38
NC_000002.11:g.96919622_96919624delinsATC , CM000664.1:g.96919622_96919624delinsATC	GRCh37
NC_000002.10:g.96283349_96283351delinsATC	NCBI36
NG_027695.1:g.17128_17130delinsGAT , LRG_528:g.17128_17130delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.639_641delinsGAT MANE Select	ENSP00000258439.3:p.Glu213=
ENST00000258439.7:c.639_641delinsGAT	ENSP00000258439.2:p.Glu213=
ENST00000432959.1:c.639_641delinsGAT	ENSP00000416660.1:p.Glu213=
ENST00000435268.1:c.387_389delinsGAT	ENSP00000411810.1:p.Glu129=
NM_001193304.2:c.639_641delinsGAT	NP_001180233.1:p.Glu213=
NM_017849.3:c.639_641delinsGAT , LRG_528t1:c.639_641delinsGAT	NP_060319.1:p.Glu213=
XM_017004450.1:c.-280_-278delinsGAT	XP_016859939.1:n.-280_-278delinsGAT
XM_017004452.1:c.387_389delinsGAT	XP_016859941.1:p.Glu129=
NM_001193304.3:c.639_641delinsGAT	NP_001180233.1:p.Glu213=
NM_017849.4:c.639_641delinsGAT MANE Select	NP_060319.1:p.Glu213=