Canonical Allele Identifier: CA1272521064
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251510A= , CM000664.2:g.96251510A= GRCh38
NC_000002.11:g.96917248A= , CM000664.1:g.96917248A= GRCh37
NC_000002.10:g.96280975A= NCBI36
NG_027695.1:g.19504T= , LRG_528:g.19504T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2298T= MANE Select ENSP00000258439.3:n.*2298T=
ENST00000258439.7:c.*2298T= ENSP00000258439.2:n.*2298T=
NM_001193304.2:c.*2298T= NP_001180233.1:n.*2298T=
NM_017849.3:c.*2298T= , LRG_528t1:c.*2298T= NP_060319.1:n.*2298T=
XM_017004450.1:c.*1599T= XP_016859939.1:n.*1599T=
XM_017004452.1:c.*2298T= XP_016859941.1:n.*2298T=
NM_001193304.3:c.*2298T= NP_001180233.1:n.*2298T=
NM_017849.4:c.*2298T= MANE Select NP_060319.1:n.*2298T=