Canonical Allele Identifier: CA1430709376

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604404C= , CM000665.2:g.194604404C=	GRCh38
NC_000003.11:g.194325133C= , CM000665.1:g.194325133C=	GRCh37
NC_000003.10:g.195806422C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1059G= MANE Select	ENSP00000333355.6:p.Thr353=
ENST00000347147.8:c.1059G=	ENSP00000333355.6:p.Thr353=
ENST00000381975.7:c.1055G=	ENSP00000371402.3:p.Arg352=
ENST00000392432.6:c.1200G=	ENSP00000376227.2:p.Thr400=
ENST00000419280.5:c.*355G=	ENSP00000414077.1:n.*355G=
ENST00000429560.1:c.251G=	ENSP00000403053.1:p.Arg84=
ENST00000432352.5:c.333G=	ENSP00000409963.1:p.Thr111=
ENST00000452358.5:c.558G=	ENSP00000414333.1:p.Thr186=
ENST00000467284.1:n.105G=
ENST00000473092.5:c.1059G=	ENSP00000418674.1:p.Thr353=
ENST00000477651.5:n.823G=
NM_001011655.2:c.1059G=	NP_001011655.1:p.Thr353=
NM_001166305.1:c.1200G=	NP_001159777.1:p.Thr400=
NM_001166306.1:c.1055G=	NP_001159778.1:p.Arg352=
NM_138399.4:c.1059G=	NP_612408.3:p.Thr353=
XM_005269371.3:c.1059G=	XP_005269428.1:p.Thr353=
XM_011513318.1:c.1209G=	XP_011511620.1:p.Thr403=
XM_011513319.1:c.1146G=	XP_011511621.1:p.Thr382=
XM_011513320.1:c.1257G=	XP_011511622.1:p.Thr419=
XM_011513321.1:c.1125G=	XP_011511623.1:p.Thr375=
XM_011513322.1:c.1116G=	XP_011511624.1:p.Thr372=
XM_011513323.1:c.954G=	XP_011511625.1:p.Thr318=
XM_005269371.4:c.1059G=	XP_005269428.1:p.Thr353=
XM_011513318.2:c.1209G=	XP_011511620.1:p.Thr403=
XM_011513319.2:c.1146G=	XP_011511621.1:p.Thr382=
XM_011513320.2:c.1257G=	XP_011511622.1:p.Thr419=
XM_011513321.2:c.1125G=	XP_011511623.1:p.Thr375=
XM_011513322.2:c.1116G=	XP_011511624.1:p.Thr372=
XM_017007517.1:c.1068G=	XP_016863006.1:p.Thr356=
XM_017007518.1:c.1068G=	XP_016863007.1:p.Thr356=
NM_001011655.3:c.1059G= MANE Select	NP_001011655.1:p.Thr353=
NM_001166305.2:c.1200G=	NP_001159777.1:p.Thr400=
NM_001166306.2:c.1055G=	NP_001159778.1:p.Arg352=
NM_138399.5:c.1059G=	NP_612408.3:p.Thr353=