Canonical Allele Identifier: CA2838795569

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254060dup , CM000664.2:g.96254060dup	GRCh38
NC_000002.11:g.96919798dup , CM000664.1:g.96919798dup	GRCh37
NC_000002.10:g.96283525dup	NCBI36
NG_027695.1:g.16955dup , LRG_528:g.16955dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.466dup MANE Select	ENSP00000258439.3:p.Ala156GlyfsTer7
ENST00000258439.7:c.466dup	ENSP00000258439.2:p.Ala156GlyfsTer7
ENST00000432959.1:c.466dup	ENSP00000416660.1:p.Ala156GlyfsTer7
ENST00000435268.1:c.214dup	ENSP00000411810.1:p.Ala72GlyfsTer7
NM_001193304.2:c.466dup	NP_001180233.1:p.Ala156GlyfsTer7
NM_017849.3:c.466dup , LRG_528t1:c.466dup	NP_060319.1:p.Ala156GlyfsTer7
XM_017004450.1:c.-453dup	XP_016859939.1:n.-453dup
XM_017004452.1:c.214dup	XP_016859941.1:p.Ala72GlyfsTer7
NM_001193304.3:c.466dup	NP_001180233.1:p.Ala156GlyfsTer7
NM_017849.4:c.466dup MANE Select	NP_060319.1:p.Ala156GlyfsTer7