Canonical Allele Identifier: CA1272522131

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254042_96254045delinsATGC , CM000664.2:g.96254042_96254045delinsATGC	GRCh38
NC_000002.11:g.96919780_96919783delinsATGC , CM000664.1:g.96919780_96919783delinsATGC	GRCh37
NC_000002.10:g.96283507_96283510delinsATGC	NCBI36
NG_027695.1:g.16969_16972delinsGCAT , LRG_528:g.16969_16972delinsGCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.480_483delinsGCAT MANE Select	ENSP00000258439.3:p.Gln160=
ENST00000258439.7:c.480_483delinsGCAT	ENSP00000258439.2:p.Gln160=
ENST00000432959.1:c.480_483delinsGCAT	ENSP00000416660.1:p.Gln160=
ENST00000435268.1:c.228_231delinsGCAT	ENSP00000411810.1:p.Gln76=
NM_001193304.2:c.480_483delinsGCAT	NP_001180233.1:p.Gln160=
NM_017849.3:c.480_483delinsGCAT , LRG_528t1:c.480_483delinsGCAT	NP_060319.1:p.Gln160=
XM_017004450.1:c.-439_-436delinsGCAT	XP_016859939.1:n.-439_-436delinsGCAT
XM_017004452.1:c.228_231delinsGCAT	XP_016859941.1:p.Gln76=
NM_001193304.3:c.480_483delinsGCAT	NP_001180233.1:p.Gln160=
NM_017849.4:c.480_483delinsGCAT MANE Select	NP_060319.1:p.Gln160=