Canonical Allele Identifier: CA1272520632
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96250599_96250601delinsTAA , CM000664.2:g.96250599_96250601delinsTAA GRCh38
NC_000002.11:g.96916337_96916339delinsTAA , CM000664.1:g.96916337_96916339delinsTAA GRCh37
NC_000002.10:g.96280064_96280066delinsTAA NCBI36
NG_027695.1:g.20413_20415delinsTTA , LRG_528:g.20413_20415delinsTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*3207_*3209delinsTTA MANE Select ENSP00000258439.3:n.*3207_*3209delinsTTA
ENST00000258439.7:c.*3207_*3209delinsTTA ENSP00000258439.2:n.*3207_*3209delinsTTA
NM_001193304.2:c.*3207_*3209delinsTTA NP_001180233.1:n.*3207_*3209delinsTTA
NM_017849.3:c.*3207_*3209delinsTTA , LRG_528t1:c.*3207_*3209delinsTTA NP_060319.1:n.*3207_*3209delinsTTA
XM_017004450.1:c.*2508_*2510delinsTTA XP_016859939.1:n.*2508_*2510delinsTTA
XM_017004452.1:c.*3207_*3209delinsTTA XP_016859941.1:n.*3207_*3209delinsTTA
NM_001193304.3:c.*3207_*3209delinsTTA NP_001180233.1:n.*3207_*3209delinsTTA
NM_017849.4:c.*3207_*3209delinsTTA MANE Select NP_060319.1:n.*3207_*3209delinsTTA