Canonical Allele Identifier: CA1272520809

Gene: TMEM127

Linked Data

• dbSNP Id: rs1684075409

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250950_96250951del , CM000664.2:g.96250950_96250951del	GRCh38
NC_000002.11:g.96916688_96916689del , CM000664.1:g.96916688_96916689del	GRCh37
NC_000002.10:g.96280415_96280416del	NCBI36
NG_027695.1:g.20063_20064del , LRG_528:g.20063_20064del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2857_*2858del MANE Select	ENSP00000258439.3:n.*2857_*2858del
ENST00000258439.7:c.*2857_*2858del	ENSP00000258439.2:n.*2857_*2858del
NM_001193304.2:c.*2857_*2858del	NP_001180233.1:n.*2857_*2858del
NM_017849.3:c.*2857_*2858del , LRG_528t1:c.*2857_*2858del	NP_060319.1:n.*2857_*2858del
XM_017004450.1:c.*2158_*2159del	XP_016859939.1:n.*2158_*2159del
XM_017004452.1:c.*2857_*2858del	XP_016859941.1:n.*2857_*2858del
NM_001193304.3:c.*2857_*2858del	NP_001180233.1:n.*2857_*2858del
NM_017849.4:c.*2857_*2858del MANE Select	NP_060319.1:n.*2857_*2858del