Canonical Allele Identifier: CA1430709428

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604442C= , CM000665.2:g.194604442C=	GRCh38
NC_000003.11:g.194325171C= , CM000665.1:g.194325171C=	GRCh37
NC_000003.10:g.195806460C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1021G= MANE Select	ENSP00000333355.6:p.Gly341=
ENST00000347147.8:c.1021G=	ENSP00000333355.6:p.Gly341=
ENST00000381975.7:c.1018-1G=	ENSP00000371402.3:n.1018-1G=
ENST00000392432.6:c.1162G=	ENSP00000376227.2:p.Gly388=
ENST00000419280.5:c.*317G=	ENSP00000414077.1:n.*317G=
ENST00000429560.1:c.214-1G=	ENSP00000403053.1:n.214-1G=
ENST00000432352.5:c.295G=	ENSP00000409963.1:p.Gly99=
ENST00000452358.5:c.520G=	ENSP00000414333.1:p.Gly174=
ENST00000467284.1:n.67G=
ENST00000473092.5:c.1021G=	ENSP00000418674.1:p.Gly341=
ENST00000477651.5:n.785G=
NM_001011655.2:c.1021G=	NP_001011655.1:p.Gly341=
NM_001166305.1:c.1162G=	NP_001159777.1:p.Gly388=
NM_001166306.1:c.1018-1G=	NP_001159778.1:n.1018-1G=
NM_138399.4:c.1021G=	NP_612408.3:p.Gly341=
XM_005269371.3:c.1021G=	XP_005269428.1:p.Gly341=
XM_011513318.1:c.1171G=	XP_011511620.1:p.Gly391=
XM_011513319.1:c.1108G=	XP_011511621.1:p.Gly370=
XM_011513320.1:c.1219G=	XP_011511622.1:p.Gly407=
XM_011513321.1:c.1087G=	XP_011511623.1:p.Gly363=
XM_011513322.1:c.1078G=	XP_011511624.1:p.Gly360=
XM_011513323.1:c.916G=	XP_011511625.1:p.Gly306=
XM_005269371.4:c.1021G=	XP_005269428.1:p.Gly341=
XM_011513318.2:c.1171G=	XP_011511620.1:p.Gly391=
XM_011513319.2:c.1108G=	XP_011511621.1:p.Gly370=
XM_011513320.2:c.1219G=	XP_011511622.1:p.Gly407=
XM_011513321.2:c.1087G=	XP_011511623.1:p.Gly363=
XM_011513322.2:c.1078G=	XP_011511624.1:p.Gly360=
XM_017007517.1:c.1030G=	XP_016863006.1:p.Gly344=
XM_017007518.1:c.1030G=	XP_016863007.1:p.Gly344=
NM_001011655.3:c.1021G= MANE Select	NP_001011655.1:p.Gly341=
NM_001166305.2:c.1162G=	NP_001159777.1:p.Gly388=
NM_001166306.2:c.1018-1G=	NP_001159778.1:n.1018-1G=
NM_138399.5:c.1021G=	NP_612408.3:p.Gly341=