Canonical Allele Identifier: CA2586964992

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254101_96254103dup , CM000664.2:g.96254101_96254103dup	GRCh38
NC_000002.11:g.96919839_96919841dup , CM000664.1:g.96919839_96919841dup	GRCh37
NC_000002.10:g.96283566_96283568dup	NCBI36
NG_027695.1:g.16913_16915dup , LRG_528:g.16913_16915dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.424_426dup MANE Select	ENSP00000258439.3:p.Thr142_Val143insThr
ENST00000258439.7:c.424_426dup	ENSP00000258439.2:p.Thr142_Val143insThr
ENST00000432959.1:c.424_426dup	ENSP00000416660.1:p.Thr142_Val143insThr
ENST00000435268.1:c.172_174dup	ENSP00000411810.1:p.Thr58_Val59insThr
NM_001193304.2:c.424_426dup	NP_001180233.1:p.Thr142_Val143insThr
NM_017849.3:c.424_426dup , LRG_528t1:c.424_426dup	NP_060319.1:p.Thr142_Val143insThr
XM_017004450.1:c.-495_-493dup	XP_016859939.1:n.-495_-493dup
XM_017004452.1:c.172_174dup	XP_016859941.1:p.Thr58_Val59insThr
NM_001193304.3:c.424_426dup	NP_001180233.1:p.Thr142_Val143insThr
NM_017849.4:c.424_426dup MANE Select	NP_060319.1:p.Thr142_Val143insThr