Canonical Allele Identifier: CA2838952699

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96265303_96265304insAG , CM000664.2:g.96265303_96265304insAG	GRCh38
NC_000002.11:g.96931041_96931042insAG , CM000664.1:g.96931041_96931042insAG	GRCh37
NC_000002.10:g.96294768_96294769insAG	NCBI36
NG_027695.1:g.5711_5712insTC , LRG_528:g.5711_5712insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.79_80insTC MANE Select	ENSP00000258439.3:p.Pro27LeufsTer?
ENST00000258439.7:c.79_80insTC	ENSP00000258439.2:p.Pro27LeufsTer?
ENST00000432959.1:c.79_80insTC	ENSP00000416660.1:p.Pro27LeufsTer?
NM_001193304.2:c.79_80insTC	NP_001180233.1:p.Pro27LeufsTer?
NM_017849.3:c.79_80insTC , LRG_528t1:c.79_80insTC	NP_060319.1:p.Pro27LeufsTer?
NM_001193304.3:c.79_80insTC	NP_001180233.1:p.Pro27LeufsTer?
NM_017849.4:c.79_80insTC MANE Select	NP_060319.1:p.Pro27LeufsTer?