Canonical Allele Identifier: CA2751314039

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251814_96251815insAA , CM000664.2:g.96251814_96251815insAA	GRCh38
NC_000002.11:g.96917552_96917553insAA , CM000664.1:g.96917552_96917553insAA	GRCh37
NC_000002.10:g.96281279_96281280insAA	NCBI36
NG_027695.1:g.19199_19200insTT , LRG_528:g.19199_19200insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*1993_*1994insTT MANE Select	ENSP00000258439.3:n.*1993_*1994insTT
ENST00000258439.7:c.*1993_*1994insTT	ENSP00000258439.2:n.*1993_*1994insTT
ENST00000432959.1:c.*1993_*1994insTT	ENSP00000416660.1:n.*1993_*1994insTT
NM_001193304.2:c.*1993_*1994insTT	NP_001180233.1:n.*1993_*1994insTT
NM_017849.3:c.*1993_*1994insTT , LRG_528t1:c.*1993_*1994insTT	NP_060319.1:n.*1993_*1994insTT
XM_017004450.1:c.*1294_*1295insTT	XP_016859939.1:n.*1294_*1295insTT
XM_017004452.1:c.*1993_*1994insTT	XP_016859941.1:n.*1993_*1994insTT
NM_001193304.3:c.*1993_*1994insTT	NP_001180233.1:n.*1993_*1994insTT
NM_017849.4:c.*1993_*1994insTT MANE Select	NP_060319.1:n.*1993_*1994insTT