Canonical Allele Identifier: CA347652701
Gene: TMEM127 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96254025G>C , CM000664.2:g.96254025G>C GRCh38
NC_000002.11:g.96919763G>C , CM000664.1:g.96919763G>C GRCh37
NC_000002.10:g.96283490G>C NCBI36
NG_027695.1:g.16989C>G , LRG_528:g.16989C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.500C>G MANE Select ENSP00000258439.3:p.Ser167Cys
ENST00000258439.7:c.500C>G ENSP00000258439.2:p.Ser167Cys
ENST00000432959.1:c.500C>G ENSP00000416660.1:p.Ser167Cys
ENST00000435268.1:c.248C>G ENSP00000411810.1:p.Ser83Cys
NM_001193304.2:c.500C>G NP_001180233.1:p.Ser167Cys
NM_017849.3:c.500C>G , LRG_528t1:c.500C>G NP_060319.1:p.Ser167Cys
XM_017004450.1:c.-419C>G XP_016859939.1:n.-419C>G
XM_017004452.1:c.248C>G XP_016859941.1:p.Ser83Cys
NM_001193304.3:c.500C>G NP_001180233.1:p.Ser167Cys
NM_017849.4:c.500C>G MANE Select NP_060319.1:p.Ser167Cys