Canonical Allele Identifier: CA2573006542
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251332dup , CM000664.2:g.96251332dup GRCh38
NC_000002.11:g.96917070dup , CM000664.1:g.96917070dup GRCh37
NC_000002.10:g.96280797dup NCBI36
NG_027695.1:g.19683dup , LRG_528:g.19683dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2477dup MANE Select ENSP00000258439.3:n.*2477dup
ENST00000258439.7:c.*2477dup ENSP00000258439.2:n.*2477dup
NM_001193304.2:c.*2477dup NP_001180233.1:n.*2477dup
NM_017849.3:c.*2477dup , LRG_528t1:c.*2477dup NP_060319.1:n.*2477dup
XM_017004450.1:c.*1778dup XP_016859939.1:n.*1778dup
XM_017004452.1:c.*2477dup XP_016859941.1:n.*2477dup
NM_001193304.3:c.*2477dup NP_001180233.1:n.*2477dup
NM_017849.4:c.*2477dup MANE Select NP_060319.1:n.*2477dup