Canonical Allele Identifier: CA347655967
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1684390081

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265209C>G , CM000664.2:g.96265209C>G GRCh38
NC_000002.11:g.96930947C>G , CM000664.1:g.96930947C>G GRCh37
NC_000002.10:g.96294674C>G NCBI36
NG_027695.1:g.5805G>C , LRG_528:g.5805G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.173G>C MANE Select ENSP00000258439.3:p.Gly58Ala
ENST00000258439.7:c.173G>C ENSP00000258439.2:p.Gly58Ala
ENST00000432959.1:c.173G>C ENSP00000416660.1:p.Gly58Ala
NM_001193304.2:c.173G>C NP_001180233.1:p.Gly58Ala
NM_017849.3:c.173G>C , LRG_528t1:c.173G>C NP_060319.1:p.Gly58Ala
NM_001193304.3:c.173G>C NP_001180233.1:p.Gly58Ala
NM_017849.4:c.173G>C MANE Select NP_060319.1:p.Gly58Ala