Canonical Allele Identifier: CA1430709368

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604400C= , CM000665.2:g.194604400C=	GRCh38
NC_000003.11:g.194325129C= , CM000665.1:g.194325129C=	GRCh37
NC_000003.10:g.195806418C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1063G= MANE Select	ENSP00000333355.6:p.Ala355=
ENST00000347147.8:c.1063G=	ENSP00000333355.6:p.Ala355=
ENST00000381975.7:c.1059G=	ENSP00000371402.3:p.Ala353=
ENST00000392432.6:c.1204G=	ENSP00000376227.2:p.Ala402=
ENST00000419280.5:c.*359G=	ENSP00000414077.1:n.*359G=
ENST00000429560.1:c.255G=	ENSP00000403053.1:p.Ala85=
ENST00000432352.5:c.337G=	ENSP00000409963.1:p.Ala113=
ENST00000452358.5:c.562G=	ENSP00000414333.1:p.Ala188=
ENST00000467284.1:n.109G=
ENST00000473092.5:c.1063G=	ENSP00000418674.1:p.Ala355=
ENST00000477651.5:n.827G=
NM_001011655.2:c.1063G=	NP_001011655.1:p.Ala355=
NM_001166305.1:c.1204G=	NP_001159777.1:p.Ala402=
NM_001166306.1:c.1059G=	NP_001159778.1:p.Ala353=
NM_138399.4:c.1063G=	NP_612408.3:p.Ala355=
XM_005269371.3:c.1063G=	XP_005269428.1:p.Ala355=
XM_011513318.1:c.1213G=	XP_011511620.1:p.Ala405=
XM_011513319.1:c.1150G=	XP_011511621.1:p.Ala384=
XM_011513320.1:c.1261G=	XP_011511622.1:p.Ala421=
XM_011513321.1:c.1129G=	XP_011511623.1:p.Ala377=
XM_011513322.1:c.1120G=	XP_011511624.1:p.Ala374=
XM_011513323.1:c.958G=	XP_011511625.1:p.Ala320=
XM_005269371.4:c.1063G=	XP_005269428.1:p.Ala355=
XM_011513318.2:c.1213G=	XP_011511620.1:p.Ala405=
XM_011513319.2:c.1150G=	XP_011511621.1:p.Ala384=
XM_011513320.2:c.1261G=	XP_011511622.1:p.Ala421=
XM_011513321.2:c.1129G=	XP_011511623.1:p.Ala377=
XM_011513322.2:c.1120G=	XP_011511624.1:p.Ala374=
XM_017007517.1:c.1072G=	XP_016863006.1:p.Ala358=
XM_017007518.1:c.1072G=	XP_016863007.1:p.Ala358=
NM_001011655.3:c.1063G= MANE Select	NP_001011655.1:p.Ala355=
NM_001166305.2:c.1204G=	NP_001159777.1:p.Ala402=
NM_001166306.2:c.1059G=	NP_001159778.1:p.Ala353=
NM_138399.5:c.1063G=	NP_612408.3:p.Ala355=