Canonical Allele Identifier: CA1272522488

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254844_96254845delinsTG , CM000664.2:g.96254844_96254845delinsTG	GRCh38
NC_000002.11:g.96920582_96920583delinsTG , CM000664.1:g.96920582_96920583delinsTG	GRCh37
NC_000002.10:g.96284309_96284310delinsTG	NCBI36
NG_027695.1:g.16169_16170delinsCA , LRG_528:g.16169_16170delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.397_398delinsCA MANE Select	ENSP00000258439.3:p.His133=
ENST00000258439.7:c.397_398delinsCA	ENSP00000258439.2:p.His133=
ENST00000432959.1:c.397_398delinsCA	ENSP00000416660.1:p.His133=
ENST00000435268.1:c.145_146delinsCA	ENSP00000411810.1:p.His49=
NM_001193304.2:c.397_398delinsCA	NP_001180233.1:p.His133=
NM_017849.3:c.397_398delinsCA , LRG_528t1:c.397_398delinsCA	NP_060319.1:p.His133=
XM_017004450.1:c.-522_-521delinsCA	XP_016859939.1:n.-522_-521delinsCA
XM_017004452.1:c.145_146delinsCA	XP_016859941.1:p.His49=
NM_001193304.3:c.397_398delinsCA	NP_001180233.1:p.His133=
NM_017849.4:c.397_398delinsCA MANE Select	NP_060319.1:p.His133=