Canonical Allele Identifier: CA1430709379

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604405G= , CM000665.2:g.194604405G=	GRCh38
NC_000003.11:g.194325134G= , CM000665.1:g.194325134G=	GRCh37
NC_000003.10:g.195806423G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1058C= MANE Select	ENSP00000333355.6:p.Thr353=
ENST00000347147.8:c.1058C=	ENSP00000333355.6:p.Thr353=
ENST00000381975.7:c.1054C=	ENSP00000371402.3:p.Arg352=
ENST00000392432.6:c.1199C=	ENSP00000376227.2:p.Thr400=
ENST00000419280.5:c.*354C=	ENSP00000414077.1:n.*354C=
ENST00000429560.1:c.250C=	ENSP00000403053.1:p.Arg84=
ENST00000432352.5:c.332C=	ENSP00000409963.1:p.Thr111=
ENST00000452358.5:c.557C=	ENSP00000414333.1:p.Thr186=
ENST00000467284.1:n.104C=
ENST00000473092.5:c.1058C=	ENSP00000418674.1:p.Thr353=
ENST00000477651.5:n.822C=
NM_001011655.2:c.1058C=	NP_001011655.1:p.Thr353=
NM_001166305.1:c.1199C=	NP_001159777.1:p.Thr400=
NM_001166306.1:c.1054C=	NP_001159778.1:p.Arg352=
NM_138399.4:c.1058C=	NP_612408.3:p.Thr353=
XM_005269371.3:c.1058C=	XP_005269428.1:p.Thr353=
XM_011513318.1:c.1208C=	XP_011511620.1:p.Thr403=
XM_011513319.1:c.1145C=	XP_011511621.1:p.Thr382=
XM_011513320.1:c.1256C=	XP_011511622.1:p.Thr419=
XM_011513321.1:c.1124C=	XP_011511623.1:p.Thr375=
XM_011513322.1:c.1115C=	XP_011511624.1:p.Thr372=
XM_011513323.1:c.953C=	XP_011511625.1:p.Thr318=
XM_005269371.4:c.1058C=	XP_005269428.1:p.Thr353=
XM_011513318.2:c.1208C=	XP_011511620.1:p.Thr403=
XM_011513319.2:c.1145C=	XP_011511621.1:p.Thr382=
XM_011513320.2:c.1256C=	XP_011511622.1:p.Thr419=
XM_011513321.2:c.1124C=	XP_011511623.1:p.Thr375=
XM_011513322.2:c.1115C=	XP_011511624.1:p.Thr372=
XM_017007517.1:c.1067C=	XP_016863006.1:p.Thr356=
XM_017007518.1:c.1067C=	XP_016863007.1:p.Thr356=
NM_001011655.3:c.1058C= MANE Select	NP_001011655.1:p.Thr353=
NM_001166305.2:c.1199C=	NP_001159777.1:p.Thr400=
NM_001166306.2:c.1054C=	NP_001159778.1:p.Arg352=
NM_138399.5:c.1058C=	NP_612408.3:p.Thr353=