Canonical Allele Identifier: CA1272527030
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265302G= , CM000664.2:g.96265302G= GRCh38
NC_000002.11:g.96931040G= , CM000664.1:g.96931040G= GRCh37
NC_000002.10:g.96294767G= NCBI36
NG_027695.1:g.5712C= , LRG_528:g.5712C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.80C= MANE Select ENSP00000258439.3:p.Pro27=
ENST00000258439.7:c.80C= ENSP00000258439.2:p.Pro27=
ENST00000432959.1:c.80C= ENSP00000416660.1:p.Pro27=
NM_001193304.2:c.80C= NP_001180233.1:p.Pro27=
NM_017849.3:c.80C= , LRG_528t1:c.80C= NP_060319.1:p.Pro27=
NM_001193304.3:c.80C= NP_001180233.1:p.Pro27=
NM_017849.4:c.80C= MANE Select NP_060319.1:p.Pro27=