Canonical Allele Identifier: CA646526651

Gene: TMEM127

Linked Data

• COSMIC: COSN15660409

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251245_96251246insT , CM000664.2:g.96251245_96251246insT	GRCh38
NC_000002.11:g.96916983_96916984insT , CM000664.1:g.96916983_96916984insT	GRCh37
NC_000002.10:g.96280710_96280711insT	NCBI36
NG_027695.1:g.19768_19769insA , LRG_528:g.19768_19769insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2562_*2563insA MANE Select	ENSP00000258439.3:n.*2562_*2563insA
ENST00000258439.7:c.*2562_*2563insA	ENSP00000258439.2:n.*2562_*2563insA
NM_001193304.2:c.*2562_*2563insA	NP_001180233.1:n.*2562_*2563insA
NM_017849.3:c.*2562_*2563insA , LRG_528t1:c.*2562_*2563insA	NP_060319.1:n.*2562_*2563insA
XM_017004450.1:c.*1863_*1864insA	XP_016859939.1:n.*1863_*1864insA
XM_017004452.1:c.*2562_*2563insA	XP_016859941.1:n.*2562_*2563insA
NM_001193304.3:c.*2562_*2563insA	NP_001180233.1:n.*2562_*2563insA
NM_017849.4:c.*2562_*2563insA MANE Select	NP_060319.1:n.*2562_*2563insA