Canonical Allele Identifier: CA1272527383
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265890G= , CM000664.2:g.96265890G= GRCh38
NC_000002.11:g.96931628G= , CM000664.1:g.96931628G= GRCh37
NC_000002.10:g.96295355G= NCBI36
NG_027695.1:g.5124C= , LRG_528:g.5124C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.-153C= MANE Select ENSP00000258439.3:n.-153C=
ENST00000258439.7:c.-153C= ENSP00000258439.2:n.-153C=
ENST00000432959.1:c.-130C= ENSP00000416660.1:n.-130C=
NM_001193304.2:c.-130C= NP_001180233.1:n.-130C=
NM_017849.3:c.-153C= , LRG_528t1:c.-153C= NP_060319.1:n.-153C=
NM_001193304.3:c.-130C= NP_001180233.1:n.-130C=
NM_017849.4:c.-153C= MANE Select NP_060319.1:n.-153C=