Canonical Allele Identifier: CA355825023
Gene: TMEM44 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.194604410C>G , CM000665.2:g.194604410C>G GRCh38
NC_000003.11:g.194325139C>G , CM000665.1:g.194325139C>G GRCh37
NC_000003.10:g.195806428C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000347147.9:c.1053G>C MANE Select ENSP00000333355.6:p.Gly351=
ENST00000347147.8:c.1053G>C ENSP00000333355.6:p.Gly351=
ENST00000381975.7:c.1049G>C ENSP00000371402.3:p.Gly350Ala
ENST00000392432.6:c.1194G>C ENSP00000376227.2:p.Gly398=
ENST00000419280.5:c.*349G>C ENSP00000414077.1:n.*349G>C
ENST00000429560.1:c.245G>C ENSP00000403053.1:p.Gly82Ala
ENST00000432352.5:c.327G>C ENSP00000409963.1:p.Gly109=
ENST00000452358.5:c.552G>C ENSP00000414333.1:p.Gly184=
ENST00000467284.1:n.99G>C
ENST00000473092.5:c.1053G>C ENSP00000418674.1:p.Gly351=
ENST00000477651.5:n.817G>C
NM_001011655.2:c.1053G>C NP_001011655.1:p.Gly351=
NM_001166305.1:c.1194G>C NP_001159777.1:p.Gly398=
NM_001166306.1:c.1049G>C NP_001159778.1:p.Gly350Ala
NM_138399.4:c.1053G>C NP_612408.3:p.Gly351=
XM_005269371.3:c.1053G>C XP_005269428.1:p.Gly351=
XM_011513318.1:c.1203G>C XP_011511620.1:p.Gly401=
XM_011513319.1:c.1140G>C XP_011511621.1:p.Gly380=
XM_011513320.1:c.1251G>C XP_011511622.1:p.Gly417=
XM_011513321.1:c.1119G>C XP_011511623.1:p.Gly373=
XM_011513322.1:c.1110G>C XP_011511624.1:p.Gly370=
XM_011513323.1:c.948G>C XP_011511625.1:p.Gly316=
XM_005269371.4:c.1053G>C XP_005269428.1:p.Gly351=
XM_011513318.2:c.1203G>C XP_011511620.1:p.Gly401=
XM_011513319.2:c.1140G>C XP_011511621.1:p.Gly380=
XM_011513320.2:c.1251G>C XP_011511622.1:p.Gly417=
XM_011513321.2:c.1119G>C XP_011511623.1:p.Gly373=
XM_011513322.2:c.1110G>C XP_011511624.1:p.Gly370=
XM_017007517.1:c.1062G>C XP_016863006.1:p.Gly354=
XM_017007518.1:c.1062G>C XP_016863007.1:p.Gly354=
NM_001011655.3:c.1053G>C MANE Select NP_001011655.1:p.Gly351=
NM_001166305.2:c.1194G>C NP_001159777.1:p.Gly398=
NM_001166306.2:c.1049G>C NP_001159778.1:p.Gly350Ala
NM_138399.5:c.1053G>C NP_612408.3:p.Gly351=