Canonical Allele Identifier: CA1272520673
Gene: TMEM127 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96250679T= , CM000664.2:g.96250679T= GRCh38
NC_000002.11:g.96916417T= , CM000664.1:g.96916417T= GRCh37
NC_000002.10:g.96280144T= NCBI36
NG_027695.1:g.20335A= , LRG_528:g.20335A=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*3129A= MANE Select ENSP00000258439.3:n.*3129A=
ENST00000258439.7:c.*3129A= ENSP00000258439.2:n.*3129A=
NM_001193304.2:c.*3129A= NP_001180233.1:n.*3129A=
NM_017849.3:c.*3129A= , LRG_528t1:c.*3129A= NP_060319.1:n.*3129A=
XM_017004450.1:c.*2430A= XP_016859939.1:n.*2430A=
XM_017004452.1:c.*3129A= XP_016859941.1:n.*3129A=
NM_001193304.3:c.*3129A= NP_001180233.1:n.*3129A=
NM_017849.4:c.*3129A= MANE Select NP_060319.1:n.*3129A=
Search 100 bp 5'
Search 100 bp 3'