Canonical Allele Identifier: CA1430709382

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604407C= , CM000665.2:g.194604407C=	GRCh38
NC_000003.11:g.194325136C= , CM000665.1:g.194325136C=	GRCh37
NC_000003.10:g.195806425C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1056G= MANE Select	ENSP00000333355.6:p.Gln352=
ENST00000347147.8:c.1056G=	ENSP00000333355.6:p.Gln352=
ENST00000381975.7:c.1052G=	ENSP00000371402.3:p.Arg351=
ENST00000392432.6:c.1197G=	ENSP00000376227.2:p.Gln399=
ENST00000419280.5:c.*352G=	ENSP00000414077.1:n.*352G=
ENST00000429560.1:c.248G=	ENSP00000403053.1:p.Arg83=
ENST00000432352.5:c.330G=	ENSP00000409963.1:p.Gln110=
ENST00000452358.5:c.555G=	ENSP00000414333.1:p.Gln185=
ENST00000467284.1:n.102G=
ENST00000473092.5:c.1056G=	ENSP00000418674.1:p.Gln352=
ENST00000477651.5:n.820G=
NM_001011655.2:c.1056G=	NP_001011655.1:p.Gln352=
NM_001166305.1:c.1197G=	NP_001159777.1:p.Gln399=
NM_001166306.1:c.1052G=	NP_001159778.1:p.Arg351=
NM_138399.4:c.1056G=	NP_612408.3:p.Gln352=
XM_005269371.3:c.1056G=	XP_005269428.1:p.Gln352=
XM_011513318.1:c.1206G=	XP_011511620.1:p.Gln402=
XM_011513319.1:c.1143G=	XP_011511621.1:p.Gln381=
XM_011513320.1:c.1254G=	XP_011511622.1:p.Gln418=
XM_011513321.1:c.1122G=	XP_011511623.1:p.Gln374=
XM_011513322.1:c.1113G=	XP_011511624.1:p.Gln371=
XM_011513323.1:c.951G=	XP_011511625.1:p.Gln317=
XM_005269371.4:c.1056G=	XP_005269428.1:p.Gln352=
XM_011513318.2:c.1206G=	XP_011511620.1:p.Gln402=
XM_011513319.2:c.1143G=	XP_011511621.1:p.Gln381=
XM_011513320.2:c.1254G=	XP_011511622.1:p.Gln418=
XM_011513321.2:c.1122G=	XP_011511623.1:p.Gln374=
XM_011513322.2:c.1113G=	XP_011511624.1:p.Gln371=
XM_017007517.1:c.1065G=	XP_016863006.1:p.Gln355=
XM_017007518.1:c.1065G=	XP_016863007.1:p.Gln355=
NM_001011655.3:c.1056G= MANE Select	NP_001011655.1:p.Gln352=
NM_001166305.2:c.1197G=	NP_001159777.1:p.Gln399=
NM_001166306.2:c.1052G=	NP_001159778.1:p.Arg351=
NM_138399.5:c.1056G=	NP_612408.3:p.Gln352=