Canonical Allele Identifier: CA1272527381
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265879G= , CM000664.2:g.96265879G= GRCh38
NC_000002.11:g.96931617G= , CM000664.1:g.96931617G= GRCh37
NC_000002.10:g.96295344G= NCBI36
NG_027695.1:g.5135C= , LRG_528:g.5135C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.-142C= MANE Select ENSP00000258439.3:n.-142C=
ENST00000258439.7:c.-142C= ENSP00000258439.2:n.-142C=
ENST00000432959.1:c.-119C= ENSP00000416660.1:n.-119C=
NM_001193304.2:c.-119C= NP_001180233.1:n.-119C=
NM_017849.3:c.-142C= , LRG_528t1:c.-142C= NP_060319.1:n.-142C=
NM_001193304.3:c.-119C= NP_001180233.1:n.-119C=
NM_017849.4:c.-142C= MANE Select NP_060319.1:n.-142C=