Canonical Allele Identifier: CA1272521472
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96252432T= , CM000664.2:g.96252432T= GRCh38
NC_000002.11:g.96918170T= , CM000664.1:g.96918170T= GRCh37
NC_000002.10:g.96281897T= NCBI36
NG_027695.1:g.18582A= , LRG_528:g.18582A=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*1376A= MANE Select ENSP00000258439.3:n.*1376A=
ENST00000258439.7:c.*1376A= ENSP00000258439.2:n.*1376A=
ENST00000432959.1:c.*1376A= ENSP00000416660.1:n.*1376A=
NM_001193304.2:c.*1376A= NP_001180233.1:n.*1376A=
NM_017849.3:c.*1376A= , LRG_528t1:c.*1376A= NP_060319.1:n.*1376A=
XM_017004450.1:c.*677A= XP_016859939.1:n.*677A=
XM_017004452.1:c.*1376A= XP_016859941.1:n.*1376A=
NM_001193304.3:c.*1376A= NP_001180233.1:n.*1376A=
NM_017849.4:c.*1376A= MANE Select NP_060319.1:n.*1376A=