Canonical Allele Identifier: CA1272522042
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1684142659

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96253888_96253889del , CM000664.2:g.96253888_96253889del GRCh38
NC_000002.11:g.96919626_96919627del , CM000664.1:g.96919626_96919627del GRCh37
NC_000002.10:g.96283353_96283354del NCBI36
NG_027695.1:g.17128_17129del , LRG_528:g.17128_17129del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.639_640del MANE Select ENSP00000258439.3:p.Glu213AspfsTer12
ENST00000258439.7:c.639_640del ENSP00000258439.2:p.Glu213AspfsTer12
ENST00000432959.1:c.639_640del ENSP00000416660.1:p.Glu213AspfsTer12
ENST00000435268.1:c.387_388del ENSP00000411810.1:p.Glu129AspfsTer12
NM_001193304.2:c.639_640del NP_001180233.1:p.Glu213AspfsTer12
NM_017849.3:c.639_640del , LRG_528t1:c.639_640del NP_060319.1:p.Glu213AspfsTer12
XM_017004450.1:c.-280_-279del XP_016859939.1:n.-280_-279del
XM_017004452.1:c.387_388del XP_016859941.1:p.Glu129AspfsTer12
NM_001193304.3:c.639_640del NP_001180233.1:p.Glu213AspfsTer12
NM_017849.4:c.639_640del MANE Select NP_060319.1:p.Glu213AspfsTer12