Canonical Allele Identifier: CA1430709318

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604378T= , CM000665.2:g.194604378T=	GRCh38
NC_000003.11:g.194325107T= , CM000665.1:g.194325107T=	GRCh37
NC_000003.10:g.195806396T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1085A= MANE Select	ENSP00000333355.6:p.Asp362=
ENST00000347147.8:c.1085A=	ENSP00000333355.6:p.Asp362=
ENST00000381975.7:c.1081A=	ENSP00000371402.3:p.Thr361=
ENST00000392432.6:c.1226A=	ENSP00000376227.2:p.Asp409=
ENST00000419280.5:c.*381A=	ENSP00000414077.1:n.*381A=
ENST00000429560.1:c.277A=	ENSP00000403053.1:p.Thr93=
ENST00000432352.5:c.359A=	ENSP00000409963.1:p.Asp120=
ENST00000452358.5:c.584A=	ENSP00000414333.1:p.Asp195=
ENST00000467284.1:n.131A=
ENST00000473092.5:c.1085A=	ENSP00000418674.1:p.Asp362=
ENST00000477651.5:n.849A=
NM_001011655.2:c.1085A=	NP_001011655.1:p.Asp362=
NM_001166305.1:c.1226A=	NP_001159777.1:p.Asp409=
NM_001166306.1:c.1081A=	NP_001159778.1:p.Thr361=
NM_138399.4:c.1085A=	NP_612408.3:p.Asp362=
XM_005269371.3:c.1085A=	XP_005269428.1:p.Asp362=
XM_011513318.1:c.1235A=	XP_011511620.1:p.Asp412=
XM_011513319.1:c.1172A=	XP_011511621.1:p.Asp391=
XM_011513320.1:c.1283A=	XP_011511622.1:p.Asp428=
XM_011513321.1:c.1151A=	XP_011511623.1:p.Asp384=
XM_011513322.1:c.1142A=	XP_011511624.1:p.Asp381=
XM_011513323.1:c.980A=	XP_011511625.1:p.Asp327=
XM_005269371.4:c.1085A=	XP_005269428.1:p.Asp362=
XM_011513318.2:c.1235A=	XP_011511620.1:p.Asp412=
XM_011513319.2:c.1172A=	XP_011511621.1:p.Asp391=
XM_011513320.2:c.1283A=	XP_011511622.1:p.Asp428=
XM_011513321.2:c.1151A=	XP_011511623.1:p.Asp384=
XM_011513322.2:c.1142A=	XP_011511624.1:p.Asp381=
XM_017007517.1:c.1094A=	XP_016863006.1:p.Asp365=
XM_017007518.1:c.1094A=	XP_016863007.1:p.Asp365=
NM_001011655.3:c.1085A= MANE Select	NP_001011655.1:p.Asp362=
NM_001166305.2:c.1226A=	NP_001159777.1:p.Asp409=
NM_001166306.2:c.1081A=	NP_001159778.1:p.Thr361=
NM_138399.5:c.1085A=	NP_612408.3:p.Asp362=