Canonical Allele Identifier: CA1272521233

Gene: TMEM127

Linked Data

• dbSNP Id: rs1684099332

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251864_96251866del , CM000664.2:g.96251864_96251866del	GRCh38
NC_000002.11:g.96917602_96917604del , CM000664.1:g.96917602_96917604del	GRCh37
NC_000002.10:g.96281329_96281331del	NCBI36
NG_027695.1:g.19150_19152del , LRG_528:g.19150_19152del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*1944_*1946del MANE Select	ENSP00000258439.3:n.*1944_*1946del
ENST00000258439.7:c.*1944_*1946del	ENSP00000258439.2:n.*1944_*1946del
ENST00000432959.1:c.*1944_*1946del	ENSP00000416660.1:n.*1944_*1946del
NM_001193304.2:c.*1944_*1946del	NP_001180233.1:n.*1944_*1946del
NM_017849.3:c.*1944_*1946del , LRG_528t1:c.*1944_*1946del	NP_060319.1:n.*1944_*1946del
XM_017004450.1:c.*1245_*1247del	XP_016859939.1:n.*1245_*1247del
XM_017004452.1:c.*1944_*1946del	XP_016859941.1:n.*1944_*1946del
NM_001193304.3:c.*1944_*1946del	NP_001180233.1:n.*1944_*1946del
NM_017849.4:c.*1944_*1946del MANE Select	NP_060319.1:n.*1944_*1946del