Canonical Allele Identifier: CA1430709272

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604361G= , CM000665.2:g.194604361G=	GRCh38
NC_000003.11:g.194325090G= , CM000665.1:g.194325090G=	GRCh37
NC_000003.10:g.195806379G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1102C= MANE Select	ENSP00000333355.6:p.Pro368=
ENST00000347147.8:c.1102C=	ENSP00000333355.6:p.Pro368=
ENST00000381975.7:c.1098C=	ENSP00000371402.3:p.Leu366=
ENST00000392432.6:c.1243C=	ENSP00000376227.2:p.Pro415=
ENST00000419280.5:c.*398C=	ENSP00000414077.1:n.*398C=
ENST00000429560.1:c.294C=	ENSP00000403053.1:p.Leu98=
ENST00000432352.5:c.376C=	ENSP00000409963.1:p.Pro126=
ENST00000452358.5:c.601C=	ENSP00000414333.1:p.Pro201=
ENST00000467284.1:n.148C=
ENST00000473092.5:c.1102C=	ENSP00000418674.1:p.Pro368=
ENST00000477651.5:n.866C=
NM_001011655.2:c.1102C=	NP_001011655.1:p.Pro368=
NM_001166305.1:c.1243C=	NP_001159777.1:p.Pro415=
NM_001166306.1:c.1098C=	NP_001159778.1:p.Leu366=
NM_138399.4:c.1102C=	NP_612408.3:p.Pro368=
XM_005269371.3:c.1102C=	XP_005269428.1:p.Pro368=
XM_011513318.1:c.1252C=	XP_011511620.1:p.Pro418=
XM_011513319.1:c.1189C=	XP_011511621.1:p.Pro397=
XM_011513320.1:c.1300C=	XP_011511622.1:p.Pro434=
XM_011513321.1:c.1168C=	XP_011511623.1:p.Pro390=
XM_011513322.1:c.1159C=	XP_011511624.1:p.Pro387=
XM_011513323.1:c.997C=	XP_011511625.1:p.Pro333=
XM_005269371.4:c.1102C=	XP_005269428.1:p.Pro368=
XM_011513318.2:c.1252C=	XP_011511620.1:p.Pro418=
XM_011513319.2:c.1189C=	XP_011511621.1:p.Pro397=
XM_011513320.2:c.1300C=	XP_011511622.1:p.Pro434=
XM_011513321.2:c.1168C=	XP_011511623.1:p.Pro390=
XM_011513322.2:c.1159C=	XP_011511624.1:p.Pro387=
XM_017007517.1:c.1111C=	XP_016863006.1:p.Pro371=
XM_017007518.1:c.1111C=	XP_016863007.1:p.Pro371=
NM_001011655.3:c.1102C= MANE Select	NP_001011655.1:p.Pro368=
NM_001166305.2:c.1243C=	NP_001159777.1:p.Pro415=
NM_001166306.2:c.1098C=	NP_001159778.1:p.Leu366=
NM_138399.5:c.1102C=	NP_612408.3:p.Pro368=