Canonical Allele Identifier: CA355825015
Gene: TMEM44 HGNC NCBI

Linked Data

dbSNP Id: rs1216220475

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.194604407C>T , CM000665.2:g.194604407C>T GRCh38
NC_000003.11:g.194325136C>T , CM000665.1:g.194325136C>T GRCh37
NC_000003.10:g.195806425C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000347147.9:c.1056G>A MANE Select ENSP00000333355.6:p.Gln352=
ENST00000347147.8:c.1056G>A ENSP00000333355.6:p.Gln352=
ENST00000381975.7:c.1052G>A ENSP00000371402.3:p.Arg351Lys
ENST00000392432.6:c.1197G>A ENSP00000376227.2:p.Gln399=
ENST00000419280.5:c.*352G>A ENSP00000414077.1:n.*352G>A
ENST00000429560.1:c.248G>A ENSP00000403053.1:p.Arg83Lys
ENST00000432352.5:c.330G>A ENSP00000409963.1:p.Gln110=
ENST00000452358.5:c.555G>A ENSP00000414333.1:p.Gln185=
ENST00000467284.1:n.102G>A
ENST00000473092.5:c.1056G>A ENSP00000418674.1:p.Gln352=
ENST00000477651.5:n.820G>A
NM_001011655.2:c.1056G>A NP_001011655.1:p.Gln352=
NM_001166305.1:c.1197G>A NP_001159777.1:p.Gln399=
NM_001166306.1:c.1052G>A NP_001159778.1:p.Arg351Lys
NM_138399.4:c.1056G>A NP_612408.3:p.Gln352=
XM_005269371.3:c.1056G>A XP_005269428.1:p.Gln352=
XM_011513318.1:c.1206G>A XP_011511620.1:p.Gln402=
XM_011513319.1:c.1143G>A XP_011511621.1:p.Gln381=
XM_011513320.1:c.1254G>A XP_011511622.1:p.Gln418=
XM_011513321.1:c.1122G>A XP_011511623.1:p.Gln374=
XM_011513322.1:c.1113G>A XP_011511624.1:p.Gln371=
XM_011513323.1:c.951G>A XP_011511625.1:p.Gln317=
XM_005269371.4:c.1056G>A XP_005269428.1:p.Gln352=
XM_011513318.2:c.1206G>A XP_011511620.1:p.Gln402=
XM_011513319.2:c.1143G>A XP_011511621.1:p.Gln381=
XM_011513320.2:c.1254G>A XP_011511622.1:p.Gln418=
XM_011513321.2:c.1122G>A XP_011511623.1:p.Gln374=
XM_011513322.2:c.1113G>A XP_011511624.1:p.Gln371=
XM_017007517.1:c.1065G>A XP_016863006.1:p.Gln355=
XM_017007518.1:c.1065G>A XP_016863007.1:p.Gln355=
NM_001011655.3:c.1056G>A MANE Select NP_001011655.1:p.Gln352=
NM_001166305.2:c.1197G>A NP_001159777.1:p.Gln399=
NM_001166306.2:c.1052G>A NP_001159778.1:p.Arg351Lys
NM_138399.5:c.1056G>A NP_612408.3:p.Gln352=