Canonical Allele Identifier: CA355825076
Gene: TMEM44 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.194604431G>C , CM000665.2:g.194604431G>C GRCh38
NC_000003.11:g.194325160G>C , CM000665.1:g.194325160G>C GRCh37
NC_000003.10:g.195806449G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000347147.9:c.1032C>G MANE Select ENSP00000333355.6:p.Ala344=
ENST00000347147.8:c.1032C>G ENSP00000333355.6:p.Ala344=
ENST00000381975.7:c.1028C>G ENSP00000371402.3:p.Pro343Arg
ENST00000392432.6:c.1173C>G ENSP00000376227.2:p.Ala391=
ENST00000419280.5:c.*328C>G ENSP00000414077.1:n.*328C>G
ENST00000429560.1:c.224C>G ENSP00000403053.1:p.Pro75Arg
ENST00000432352.5:c.306C>G ENSP00000409963.1:p.Ala102=
ENST00000452358.5:c.531C>G ENSP00000414333.1:p.Ala177=
ENST00000467284.1:n.78C>G
ENST00000473092.5:c.1032C>G ENSP00000418674.1:p.Ala344=
ENST00000477651.5:n.796C>G
NM_001011655.2:c.1032C>G NP_001011655.1:p.Ala344=
NM_001166305.1:c.1173C>G NP_001159777.1:p.Ala391=
NM_001166306.1:c.1028C>G NP_001159778.1:p.Pro343Arg
NM_138399.4:c.1032C>G NP_612408.3:p.Ala344=
XM_005269371.3:c.1032C>G XP_005269428.1:p.Ala344=
XM_011513318.1:c.1182C>G XP_011511620.1:p.Ala394=
XM_011513319.1:c.1119C>G XP_011511621.1:p.Ala373=
XM_011513320.1:c.1230C>G XP_011511622.1:p.Ala410=
XM_011513321.1:c.1098C>G XP_011511623.1:p.Ala366=
XM_011513322.1:c.1089C>G XP_011511624.1:p.Ala363=
XM_011513323.1:c.927C>G XP_011511625.1:p.Ala309=
XM_005269371.4:c.1032C>G XP_005269428.1:p.Ala344=
XM_011513318.2:c.1182C>G XP_011511620.1:p.Ala394=
XM_011513319.2:c.1119C>G XP_011511621.1:p.Ala373=
XM_011513320.2:c.1230C>G XP_011511622.1:p.Ala410=
XM_011513321.2:c.1098C>G XP_011511623.1:p.Ala366=
XM_011513322.2:c.1089C>G XP_011511624.1:p.Ala363=
XM_017007517.1:c.1041C>G XP_016863006.1:p.Ala347=
XM_017007518.1:c.1041C>G XP_016863007.1:p.Ala347=
NM_001011655.3:c.1032C>G MANE Select NP_001011655.1:p.Ala344=
NM_001166305.2:c.1173C>G NP_001159777.1:p.Ala391=
NM_001166306.2:c.1028C>G NP_001159778.1:p.Pro343Arg
NM_138399.5:c.1032C>G NP_612408.3:p.Ala344=