Canonical Allele Identifier: CA1272520854

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251065_96251066delinsAG , CM000664.2:g.96251065_96251066delinsAG	GRCh38
NC_000002.11:g.96916803_96916804delinsAG , CM000664.1:g.96916803_96916804delinsAG	GRCh37
NC_000002.10:g.96280530_96280531delinsAG	NCBI36
NG_027695.1:g.19948_19949delinsCT , LRG_528:g.19948_19949delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2742_*2743delinsCT MANE Select	ENSP00000258439.3:n.*2742_*2743delinsCT
ENST00000258439.7:c.*2742_*2743delinsCT	ENSP00000258439.2:n.*2742_*2743delinsCT
NM_001193304.2:c.*2742_*2743delinsCT	NP_001180233.1:n.*2742_*2743delinsCT
NM_017849.3:c.*2742_*2743delinsCT , LRG_528t1:c.*2742_*2743delinsCT	NP_060319.1:n.*2742_*2743delinsCT
XM_017004450.1:c.*2043_*2044delinsCT	XP_016859939.1:n.*2043_*2044delinsCT
XM_017004452.1:c.*2742_*2743delinsCT	XP_016859941.1:n.*2742_*2743delinsCT
NM_001193304.3:c.*2742_*2743delinsCT	NP_001180233.1:n.*2742_*2743delinsCT
NM_017849.4:c.*2742_*2743delinsCT MANE Select	NP_060319.1:n.*2742_*2743delinsCT