Canonical Allele Identifier: CA347652819
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs2104285018

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96254044G>A , CM000664.2:g.96254044G>A GRCh38
NC_000002.11:g.96919782G>A , CM000664.1:g.96919782G>A GRCh37
NC_000002.10:g.96283509G>A NCBI36
NG_027695.1:g.16970C>T , LRG_528:g.16970C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.481C>T MANE Select ENSP00000258439.3:p.His161Tyr
ENST00000258439.7:c.481C>T ENSP00000258439.2:p.His161Tyr
ENST00000432959.1:c.481C>T ENSP00000416660.1:p.His161Tyr
ENST00000435268.1:c.229C>T ENSP00000411810.1:p.His77Tyr
NM_001193304.2:c.481C>T NP_001180233.1:p.His161Tyr
NM_017849.3:c.481C>T , LRG_528t1:c.481C>T NP_060319.1:p.His161Tyr
XM_017004450.1:c.-438C>T XP_016859939.1:n.-438C>T
XM_017004452.1:c.229C>T XP_016859941.1:p.His77Tyr
NM_001193304.3:c.481C>T NP_001180233.1:p.His161Tyr
NM_017849.4:c.481C>T MANE Select NP_060319.1:p.His161Tyr