Canonical Allele Identifier: CA1430709372

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604401G= , CM000665.2:g.194604401G=	GRCh38
NC_000003.11:g.194325130G= , CM000665.1:g.194325130G=	GRCh37
NC_000003.10:g.195806419G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1062C= MANE Select	ENSP00000333355.6:p.Ser354=
ENST00000347147.8:c.1062C=	ENSP00000333355.6:p.Ser354=
ENST00000381975.7:c.1058C=	ENSP00000371402.3:p.Ala353=
ENST00000392432.6:c.1203C=	ENSP00000376227.2:p.Ser401=
ENST00000419280.5:c.*358C=	ENSP00000414077.1:n.*358C=
ENST00000429560.1:c.254C=	ENSP00000403053.1:p.Ala85=
ENST00000432352.5:c.336C=	ENSP00000409963.1:p.Ser112=
ENST00000452358.5:c.561C=	ENSP00000414333.1:p.Ser187=
ENST00000467284.1:n.108C=
ENST00000473092.5:c.1062C=	ENSP00000418674.1:p.Ser354=
ENST00000477651.5:n.826C=
NM_001011655.2:c.1062C=	NP_001011655.1:p.Ser354=
NM_001166305.1:c.1203C=	NP_001159777.1:p.Ser401=
NM_001166306.1:c.1058C=	NP_001159778.1:p.Ala353=
NM_138399.4:c.1062C=	NP_612408.3:p.Ser354=
XM_005269371.3:c.1062C=	XP_005269428.1:p.Ser354=
XM_011513318.1:c.1212C=	XP_011511620.1:p.Ser404=
XM_011513319.1:c.1149C=	XP_011511621.1:p.Ser383=
XM_011513320.1:c.1260C=	XP_011511622.1:p.Ser420=
XM_011513321.1:c.1128C=	XP_011511623.1:p.Ser376=
XM_011513322.1:c.1119C=	XP_011511624.1:p.Ser373=
XM_011513323.1:c.957C=	XP_011511625.1:p.Ser319=
XM_005269371.4:c.1062C=	XP_005269428.1:p.Ser354=
XM_011513318.2:c.1212C=	XP_011511620.1:p.Ser404=
XM_011513319.2:c.1149C=	XP_011511621.1:p.Ser383=
XM_011513320.2:c.1260C=	XP_011511622.1:p.Ser420=
XM_011513321.2:c.1128C=	XP_011511623.1:p.Ser376=
XM_011513322.2:c.1119C=	XP_011511624.1:p.Ser373=
XM_017007517.1:c.1071C=	XP_016863006.1:p.Ser357=
XM_017007518.1:c.1071C=	XP_016863007.1:p.Ser357=
NM_001011655.3:c.1062C= MANE Select	NP_001011655.1:p.Ser354=
NM_001166305.2:c.1203C=	NP_001159777.1:p.Ser401=
NM_001166306.2:c.1058C=	NP_001159778.1:p.Ala353=
NM_138399.5:c.1062C=	NP_612408.3:p.Ser354=