Canonical Allele Identifier: CA355825037
Gene: TMEM44 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.194604416A>T , CM000665.2:g.194604416A>T GRCh38
NC_000003.11:g.194325145A>T , CM000665.1:g.194325145A>T GRCh37
NC_000003.10:g.195806434A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000347147.9:c.1047T>A MANE Select ENSP00000333355.6:p.Gly349=
ENST00000347147.8:c.1047T>A ENSP00000333355.6:p.Gly349=
ENST00000381975.7:c.1043T>A ENSP00000371402.3:p.Val348Glu
ENST00000392432.6:c.1188T>A ENSP00000376227.2:p.Gly396=
ENST00000419280.5:c.*343T>A ENSP00000414077.1:n.*343T>A
ENST00000429560.1:c.239T>A ENSP00000403053.1:p.Val80Glu
ENST00000432352.5:c.321T>A ENSP00000409963.1:p.Gly107=
ENST00000452358.5:c.546T>A ENSP00000414333.1:p.Gly182=
ENST00000467284.1:n.93T>A
ENST00000473092.5:c.1047T>A ENSP00000418674.1:p.Gly349=
ENST00000477651.5:n.811T>A
NM_001011655.2:c.1047T>A NP_001011655.1:p.Gly349=
NM_001166305.1:c.1188T>A NP_001159777.1:p.Gly396=
NM_001166306.1:c.1043T>A NP_001159778.1:p.Val348Glu
NM_138399.4:c.1047T>A NP_612408.3:p.Gly349=
XM_005269371.3:c.1047T>A XP_005269428.1:p.Gly349=
XM_011513318.1:c.1197T>A XP_011511620.1:p.Gly399=
XM_011513319.1:c.1134T>A XP_011511621.1:p.Gly378=
XM_011513320.1:c.1245T>A XP_011511622.1:p.Gly415=
XM_011513321.1:c.1113T>A XP_011511623.1:p.Gly371=
XM_011513322.1:c.1104T>A XP_011511624.1:p.Gly368=
XM_011513323.1:c.942T>A XP_011511625.1:p.Gly314=
XM_005269371.4:c.1047T>A XP_005269428.1:p.Gly349=
XM_011513318.2:c.1197T>A XP_011511620.1:p.Gly399=
XM_011513319.2:c.1134T>A XP_011511621.1:p.Gly378=
XM_011513320.2:c.1245T>A XP_011511622.1:p.Gly415=
XM_011513321.2:c.1113T>A XP_011511623.1:p.Gly371=
XM_011513322.2:c.1104T>A XP_011511624.1:p.Gly368=
XM_017007517.1:c.1056T>A XP_016863006.1:p.Gly352=
XM_017007518.1:c.1056T>A XP_016863007.1:p.Gly352=
NM_001011655.3:c.1047T>A MANE Select NP_001011655.1:p.Gly349=
NM_001166305.2:c.1188T>A NP_001159777.1:p.Gly396=
NM_001166306.2:c.1043T>A NP_001159778.1:p.Val348Glu
NM_138399.5:c.1047T>A NP_612408.3:p.Gly349=