Canonical Allele Identifier: CA1272522171
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96254127_96254128delinsAG , CM000664.2:g.96254127_96254128delinsAG GRCh38
NC_000002.11:g.96919865_96919866delinsAG , CM000664.1:g.96919865_96919866delinsAG GRCh37
NC_000002.10:g.96283592_96283593delinsAG NCBI36
NG_027695.1:g.16886_16887delinsCT , LRG_528:g.16886_16887delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.410-13_410-12delinsCT MANE Select ENSP00000258439.3:n.410-13_410-12delinsCT...
ENST00000258439.7:c.410-13_410-12delinsCT ENSP00000258439.2:n.410-13_410-12delinsCT...
ENST00000432959.1:c.410-13_410-12delinsCT ENSP00000416660.1:n.410-13_410-12delinsCT...
ENST00000435268.1:c.158-13_158-12delinsCT ENSP00000411810.1:n.158-13_158-12delinsCT...
NM_001193304.2:c.410-13_410-12delinsCT NP_001180233.1:n.410-13_410-12delinsCT
NM_017849.3:c.410-13_410-12delinsCT , LRG_528t1:c.410-13_410-12delinsCT NP_060319.1:n.410-13_410-12delinsCT
XM_017004450.1:c.-509-13_-509-12delinsCT XP_016859939.1:n.-509-13_-509-12delinsCT
XM_017004452.1:c.158-13_158-12delinsCT XP_016859941.1:n.158-13_158-12delinsCT
NM_001193304.3:c.410-13_410-12delinsCT NP_001180233.1:n.410-13_410-12delinsCT
NM_017849.4:c.410-13_410-12delinsCT MANE Select NP_060319.1:n.410-13_410-12delinsCT