Canonical Allele Identifier: CA1430709334

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604388A= , CM000665.2:g.194604388A=	GRCh38
NC_000003.11:g.194325117A= , CM000665.1:g.194325117A=	GRCh37
NC_000003.10:g.195806406A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1075T= MANE Select	ENSP00000333355.6:p.Ser359=
ENST00000347147.8:c.1075T=	ENSP00000333355.6:p.Ser359=
ENST00000381975.7:c.1071T=	ENSP00000371402.3:p.Arg357=
ENST00000392432.6:c.1216T=	ENSP00000376227.2:p.Ser406=
ENST00000419280.5:c.*371T=	ENSP00000414077.1:n.*371T=
ENST00000429560.1:c.267T=	ENSP00000403053.1:p.Arg89=
ENST00000432352.5:c.349T=	ENSP00000409963.1:p.Ser117=
ENST00000452358.5:c.574T=	ENSP00000414333.1:p.Ser192=
ENST00000467284.1:n.121T=
ENST00000473092.5:c.1075T=	ENSP00000418674.1:p.Ser359=
ENST00000477651.5:n.839T=
NM_001011655.2:c.1075T=	NP_001011655.1:p.Ser359=
NM_001166305.1:c.1216T=	NP_001159777.1:p.Ser406=
NM_001166306.1:c.1071T=	NP_001159778.1:p.Arg357=
NM_138399.4:c.1075T=	NP_612408.3:p.Ser359=
XM_005269371.3:c.1075T=	XP_005269428.1:p.Ser359=
XM_011513318.1:c.1225T=	XP_011511620.1:p.Ser409=
XM_011513319.1:c.1162T=	XP_011511621.1:p.Ser388=
XM_011513320.1:c.1273T=	XP_011511622.1:p.Ser425=
XM_011513321.1:c.1141T=	XP_011511623.1:p.Ser381=
XM_011513322.1:c.1132T=	XP_011511624.1:p.Ser378=
XM_011513323.1:c.970T=	XP_011511625.1:p.Ser324=
XM_005269371.4:c.1075T=	XP_005269428.1:p.Ser359=
XM_011513318.2:c.1225T=	XP_011511620.1:p.Ser409=
XM_011513319.2:c.1162T=	XP_011511621.1:p.Ser388=
XM_011513320.2:c.1273T=	XP_011511622.1:p.Ser425=
XM_011513321.2:c.1141T=	XP_011511623.1:p.Ser381=
XM_011513322.2:c.1132T=	XP_011511624.1:p.Ser378=
XM_017007517.1:c.1084T=	XP_016863006.1:p.Ser362=
XM_017007518.1:c.1084T=	XP_016863007.1:p.Ser362=
NM_001011655.3:c.1075T= MANE Select	NP_001011655.1:p.Ser359=
NM_001166305.2:c.1216T=	NP_001159777.1:p.Ser406=
NM_001166306.2:c.1071T=	NP_001159778.1:p.Arg357=
NM_138399.5:c.1075T=	NP_612408.3:p.Ser359=