Canonical Allele Identifier: CA1430709291

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604370A= , CM000665.2:g.194604370A=	GRCh38
NC_000003.11:g.194325099A= , CM000665.1:g.194325099A=	GRCh37
NC_000003.10:g.195806388A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1093T= MANE Select	ENSP00000333355.6:p.Ser365=
ENST00000347147.8:c.1093T=	ENSP00000333355.6:p.Ser365=
ENST00000381975.7:c.1089T=	ENSP00000371402.3:p.Arg363=
ENST00000392432.6:c.1234T=	ENSP00000376227.2:p.Ser412=
ENST00000419280.5:c.*389T=	ENSP00000414077.1:n.*389T=
ENST00000429560.1:c.285T=	ENSP00000403053.1:p.Arg95=
ENST00000432352.5:c.367T=	ENSP00000409963.1:p.Ser123=
ENST00000452358.5:c.592T=	ENSP00000414333.1:p.Ser198=
ENST00000467284.1:n.139T=
ENST00000473092.5:c.1093T=	ENSP00000418674.1:p.Ser365=
ENST00000477651.5:n.857T=
NM_001011655.2:c.1093T=	NP_001011655.1:p.Ser365=
NM_001166305.1:c.1234T=	NP_001159777.1:p.Ser412=
NM_001166306.1:c.1089T=	NP_001159778.1:p.Arg363=
NM_138399.4:c.1093T=	NP_612408.3:p.Ser365=
XM_005269371.3:c.1093T=	XP_005269428.1:p.Ser365=
XM_011513318.1:c.1243T=	XP_011511620.1:p.Ser415=
XM_011513319.1:c.1180T=	XP_011511621.1:p.Ser394=
XM_011513320.1:c.1291T=	XP_011511622.1:p.Ser431=
XM_011513321.1:c.1159T=	XP_011511623.1:p.Ser387=
XM_011513322.1:c.1150T=	XP_011511624.1:p.Ser384=
XM_011513323.1:c.988T=	XP_011511625.1:p.Ser330=
XM_005269371.4:c.1093T=	XP_005269428.1:p.Ser365=
XM_011513318.2:c.1243T=	XP_011511620.1:p.Ser415=
XM_011513319.2:c.1180T=	XP_011511621.1:p.Ser394=
XM_011513320.2:c.1291T=	XP_011511622.1:p.Ser431=
XM_011513321.2:c.1159T=	XP_011511623.1:p.Ser387=
XM_011513322.2:c.1150T=	XP_011511624.1:p.Ser384=
XM_017007517.1:c.1102T=	XP_016863006.1:p.Ser368=
XM_017007518.1:c.1102T=	XP_016863007.1:p.Ser368=
NM_001011655.3:c.1093T= MANE Select	NP_001011655.1:p.Ser365=
NM_001166305.2:c.1234T=	NP_001159777.1:p.Ser412=
NM_001166306.2:c.1089T=	NP_001159778.1:p.Arg363=
NM_138399.5:c.1093T=	NP_612408.3:p.Ser365=