Canonical Allele Identifier: CA1430709516
Gene: TMEM44 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.194604570_194604571delinsTG , CM000665.2:g.194604570_194604571delinsTG GRCh38
NC_000003.11:g.194325299_194325300delinsTG , CM000665.1:g.194325299_194325300delinsTG GRCh37
NC_000003.10:g.195806588_195806589delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000347147.9:c.1018-126_1018-125delinsCA MANE Select ENSP00000333355.6:n.1018-126_1018-125delinsCA
ENST00000347147.8:c.1018-126_1018-125delinsCA ENSP00000333355.6:n.1018-126_1018-125delinsCA
ENST00000381975.7:c.1018-130_1018-129delinsCA ENSP00000371402.3:n.1018-130_1018-129delinsCA
ENST00000392432.6:c.1159-126_1159-125delinsCA ENSP00000376227.2:n.1159-126_1159-125delinsCA
ENST00000419280.5:c.*314-126_*314-125delinsCA ENSP00000414077.1:n.*314-126_*314-125delinsCA
ENST00000429560.1:c.214-130_214-129delinsCA ENSP00000403053.1:n.214-130_214-129delinsCA
ENST00000432352.5:c.292-126_292-125delinsCA ENSP00000409963.1:n.292-126_292-125delinsCA
ENST00000452358.5:c.517-126_517-125delinsCA ENSP00000414333.1:n.517-126_517-125delinsCA
ENST00000467284.1:n.64-126_64-125delinsCA
ENST00000473092.5:c.1018-126_1018-125delinsCA ENSP00000418674.1:n.1018-126_1018-125delinsCA
ENST00000477651.5:n.782-126_782-125delinsCA
NM_001011655.2:c.1018-126_1018-125delinsCA NP_001011655.1:n.1018-126_1018-125delinsCA
NM_001166305.1:c.1159-126_1159-125delinsCA NP_001159777.1:n.1159-126_1159-125delinsCA
NM_001166306.1:c.1018-130_1018-129delinsCA NP_001159778.1:n.1018-130_1018-129delinsCA
NM_138399.4:c.1018-126_1018-125delinsCA NP_612408.3:n.1018-126_1018-125delinsCA
XM_005269371.3:c.1018-126_1018-125delinsCA XP_005269428.1:n.1018-126_1018-125delinsCA
XM_011513318.1:c.1168-126_1168-125delinsCA XP_011511620.1:n.1168-126_1168-125delinsCA
XM_011513319.1:c.1105-126_1105-125delinsCA XP_011511621.1:n.1105-126_1105-125delinsCA
XM_011513320.1:c.1216-126_1216-125delinsCA XP_011511622.1:n.1216-126_1216-125delinsCA
XM_011513321.1:c.1084-126_1084-125delinsCA XP_011511623.1:n.1084-126_1084-125delinsCA
XM_011513322.1:c.1075-126_1075-125delinsCA XP_011511624.1:n.1075-126_1075-125delinsCA
XM_011513323.1:c.913-126_913-125delinsCA XP_011511625.1:n.913-126_913-125delinsCA
XM_005269371.4:c.1018-126_1018-125delinsCA XP_005269428.1:n.1018-126_1018-125delinsCA
XM_011513318.2:c.1168-126_1168-125delinsCA XP_011511620.1:n.1168-126_1168-125delinsCA
XM_011513319.2:c.1105-126_1105-125delinsCA XP_011511621.1:n.1105-126_1105-125delinsCA
XM_011513320.2:c.1216-126_1216-125delinsCA XP_011511622.1:n.1216-126_1216-125delinsCA
XM_011513321.2:c.1084-126_1084-125delinsCA XP_011511623.1:n.1084-126_1084-125delinsCA
XM_011513322.2:c.1075-126_1075-125delinsCA XP_011511624.1:n.1075-126_1075-125delinsCA
XM_017007517.1:c.1027-126_1027-125delinsCA XP_016863006.1:n.1027-126_1027-125delinsCA
XM_017007518.1:c.1027-126_1027-125delinsCA XP_016863007.1:n.1027-126_1027-125delinsCA
NM_001011655.3:c.1018-126_1018-125delinsCA MANE Select NP_001011655.1:n.1018-126_1018-125delinsCA
NM_001166305.2:c.1159-126_1159-125delinsCA NP_001159777.1:n.1159-126_1159-125delinsCA
NM_001166306.2:c.1018-130_1018-129delinsCA NP_001159778.1:n.1018-130_1018-129delinsCA
NM_138399.5:c.1018-126_1018-125delinsCA NP_612408.3:n.1018-126_1018-125delinsCA