Canonical Allele Identifier: CA1430709284

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604368C= , CM000665.2:g.194604368C=	GRCh38
NC_000003.11:g.194325097C= , CM000665.1:g.194325097C=	GRCh37
NC_000003.10:g.195806386C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1095G= MANE Select	ENSP00000333355.6:p.Ser365=
ENST00000347147.8:c.1095G=	ENSP00000333355.6:p.Ser365=
ENST00000381975.7:c.1091G=	ENSP00000371402.3:p.Arg364=
ENST00000392432.6:c.1236G=	ENSP00000376227.2:p.Ser412=
ENST00000419280.5:c.*391G=	ENSP00000414077.1:n.*391G=
ENST00000429560.1:c.287G=	ENSP00000403053.1:p.Arg96=
ENST00000432352.5:c.369G=	ENSP00000409963.1:p.Ser123=
ENST00000452358.5:c.594G=	ENSP00000414333.1:p.Ser198=
ENST00000467284.1:n.141G=
ENST00000473092.5:c.1095G=	ENSP00000418674.1:p.Ser365=
ENST00000477651.5:n.859G=
NM_001011655.2:c.1095G=	NP_001011655.1:p.Ser365=
NM_001166305.1:c.1236G=	NP_001159777.1:p.Ser412=
NM_001166306.1:c.1091G=	NP_001159778.1:p.Arg364=
NM_138399.4:c.1095G=	NP_612408.3:p.Ser365=
XM_005269371.3:c.1095G=	XP_005269428.1:p.Ser365=
XM_011513318.1:c.1245G=	XP_011511620.1:p.Ser415=
XM_011513319.1:c.1182G=	XP_011511621.1:p.Ser394=
XM_011513320.1:c.1293G=	XP_011511622.1:p.Ser431=
XM_011513321.1:c.1161G=	XP_011511623.1:p.Ser387=
XM_011513322.1:c.1152G=	XP_011511624.1:p.Ser384=
XM_011513323.1:c.990G=	XP_011511625.1:p.Ser330=
XM_005269371.4:c.1095G=	XP_005269428.1:p.Ser365=
XM_011513318.2:c.1245G=	XP_011511620.1:p.Ser415=
XM_011513319.2:c.1182G=	XP_011511621.1:p.Ser394=
XM_011513320.2:c.1293G=	XP_011511622.1:p.Ser431=
XM_011513321.2:c.1161G=	XP_011511623.1:p.Ser387=
XM_011513322.2:c.1152G=	XP_011511624.1:p.Ser384=
XM_017007517.1:c.1104G=	XP_016863006.1:p.Ser368=
XM_017007518.1:c.1104G=	XP_016863007.1:p.Ser368=
NM_001011655.3:c.1095G= MANE Select	NP_001011655.1:p.Ser365=
NM_001166305.2:c.1236G=	NP_001159777.1:p.Ser412=
NM_001166306.2:c.1091G=	NP_001159778.1:p.Arg364=
NM_138399.5:c.1095G=	NP_612408.3:p.Ser365=