Canonical Allele Identifier: CA355825053
Gene: TMEM44 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.194604422C>T , CM000665.2:g.194604422C>T GRCh38
NC_000003.11:g.194325151C>T , CM000665.1:g.194325151C>T GRCh37
NC_000003.10:g.195806440C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000347147.9:c.1041G>A MANE Select ENSP00000333355.6:p.Leu347=
ENST00000347147.8:c.1041G>A ENSP00000333355.6:p.Leu347=
ENST00000381975.7:c.1037G>A ENSP00000371402.3:p.Cys346Tyr
ENST00000392432.6:c.1182G>A ENSP00000376227.2:p.Leu394=
ENST00000419280.5:c.*337G>A ENSP00000414077.1:n.*337G>A
ENST00000429560.1:c.233G>A ENSP00000403053.1:p.Cys78Tyr
ENST00000432352.5:c.315G>A ENSP00000409963.1:p.Leu105=
ENST00000452358.5:c.540G>A ENSP00000414333.1:p.Leu180=
ENST00000467284.1:n.87G>A
ENST00000473092.5:c.1041G>A ENSP00000418674.1:p.Leu347=
ENST00000477651.5:n.805G>A
NM_001011655.2:c.1041G>A NP_001011655.1:p.Leu347=
NM_001166305.1:c.1182G>A NP_001159777.1:p.Leu394=
NM_001166306.1:c.1037G>A NP_001159778.1:p.Cys346Tyr
NM_138399.4:c.1041G>A NP_612408.3:p.Leu347=
XM_005269371.3:c.1041G>A XP_005269428.1:p.Leu347=
XM_011513318.1:c.1191G>A XP_011511620.1:p.Leu397=
XM_011513319.1:c.1128G>A XP_011511621.1:p.Leu376=
XM_011513320.1:c.1239G>A XP_011511622.1:p.Leu413=
XM_011513321.1:c.1107G>A XP_011511623.1:p.Leu369=
XM_011513322.1:c.1098G>A XP_011511624.1:p.Leu366=
XM_011513323.1:c.936G>A XP_011511625.1:p.Leu312=
XM_005269371.4:c.1041G>A XP_005269428.1:p.Leu347=
XM_011513318.2:c.1191G>A XP_011511620.1:p.Leu397=
XM_011513319.2:c.1128G>A XP_011511621.1:p.Leu376=
XM_011513320.2:c.1239G>A XP_011511622.1:p.Leu413=
XM_011513321.2:c.1107G>A XP_011511623.1:p.Leu369=
XM_011513322.2:c.1098G>A XP_011511624.1:p.Leu366=
XM_017007517.1:c.1050G>A XP_016863006.1:p.Leu350=
XM_017007518.1:c.1050G>A XP_016863007.1:p.Leu350=
NM_001011655.3:c.1041G>A MANE Select NP_001011655.1:p.Leu347=
NM_001166305.2:c.1182G>A NP_001159777.1:p.Leu394=
NM_001166306.2:c.1037G>A NP_001159778.1:p.Cys346Tyr
NM_138399.5:c.1041G>A NP_612408.3:p.Leu347=