Canonical Allele Identifier: CA2699676146

Gene: TMEM127

Linked Data

• dbSNP Id: rs777748763

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254051_96254056del , CM000664.2:g.96254051_96254056del	GRCh38
NC_000002.11:g.96919789_96919794del , CM000664.1:g.96919789_96919794del	GRCh37
NC_000002.10:g.96283516_96283521del	NCBI36
NG_027695.1:g.16966_16971del , LRG_528:g.16966_16971del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.477_482del MANE Select	ENSP00000258439.3:p.Gln159_Gln160del
ENST00000258439.7:c.477_482del	ENSP00000258439.2:p.Gln159_Gln160del
ENST00000432959.1:c.477_482del	ENSP00000416660.1:p.Gln159_Gln160del
ENST00000435268.1:c.225_230del	ENSP00000411810.1:p.Gln75_Gln76del
NM_001193304.2:c.477_482del	NP_001180233.1:p.Gln159_Gln160del
NM_017849.3:c.477_482del , LRG_528t1:c.477_482del	NP_060319.1:p.Gln159_Gln160del
XM_017004450.1:c.-442_-437del	XP_016859939.1:n.-442_-437del
XM_017004452.1:c.225_230del	XP_016859941.1:p.Gln75_Gln76del
NM_001193304.3:c.477_482del	NP_001180233.1:p.Gln159_Gln160del
NM_017849.4:c.477_482del MANE Select	NP_060319.1:p.Gln159_Gln160del