Canonical Allele Identifier: CA355825103
Gene: TMEM44 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.194604440G>T , CM000665.2:g.194604440G>T GRCh38
NC_000003.11:g.194325169G>T , CM000665.1:g.194325169G>T GRCh37
NC_000003.10:g.195806458G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000347147.9:c.1023C>A MANE Select ENSP00000333355.6:p.Gly341=
ENST00000347147.8:c.1023C>A ENSP00000333355.6:p.Gly341=
ENST00000381975.7:c.1019C>A ENSP00000371402.3:p.Ala340Asp
ENST00000392432.6:c.1164C>A ENSP00000376227.2:p.Gly388=
ENST00000419280.5:c.*319C>A ENSP00000414077.1:n.*319C>A
ENST00000429560.1:c.215C>A ENSP00000403053.1:p.Ala72Asp
ENST00000432352.5:c.297C>A ENSP00000409963.1:p.Gly99=
ENST00000452358.5:c.522C>A ENSP00000414333.1:p.Gly174=
ENST00000467284.1:n.69C>A
ENST00000473092.5:c.1023C>A ENSP00000418674.1:p.Gly341=
ENST00000477651.5:n.787C>A
NM_001011655.2:c.1023C>A NP_001011655.1:p.Gly341=
NM_001166305.1:c.1164C>A NP_001159777.1:p.Gly388=
NM_001166306.1:c.1019C>A NP_001159778.1:p.Ala340Asp
NM_138399.4:c.1023C>A NP_612408.3:p.Gly341=
XM_005269371.3:c.1023C>A XP_005269428.1:p.Gly341=
XM_011513318.1:c.1173C>A XP_011511620.1:p.Gly391=
XM_011513319.1:c.1110C>A XP_011511621.1:p.Gly370=
XM_011513320.1:c.1221C>A XP_011511622.1:p.Gly407=
XM_011513321.1:c.1089C>A XP_011511623.1:p.Gly363=
XM_011513322.1:c.1080C>A XP_011511624.1:p.Gly360=
XM_011513323.1:c.918C>A XP_011511625.1:p.Gly306=
XM_005269371.4:c.1023C>A XP_005269428.1:p.Gly341=
XM_011513318.2:c.1173C>A XP_011511620.1:p.Gly391=
XM_011513319.2:c.1110C>A XP_011511621.1:p.Gly370=
XM_011513320.2:c.1221C>A XP_011511622.1:p.Gly407=
XM_011513321.2:c.1089C>A XP_011511623.1:p.Gly363=
XM_011513322.2:c.1080C>A XP_011511624.1:p.Gly360=
XM_017007517.1:c.1032C>A XP_016863006.1:p.Gly344=
XM_017007518.1:c.1032C>A XP_016863007.1:p.Gly344=
NM_001011655.3:c.1023C>A MANE Select NP_001011655.1:p.Gly341=
NM_001166305.2:c.1164C>A NP_001159777.1:p.Gly388=
NM_001166306.2:c.1019C>A NP_001159778.1:p.Ala340Asp
NM_138399.5:c.1023C>A NP_612408.3:p.Gly341=