Canonical Allele Identifier: CA355825005

Gene: TMEM44

Linked Data

• MyVariant Identifiers: chr3:g.194325132T>G (hg19) ; chr3:g.194604403T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604403T>G , CM000665.2:g.194604403T>G	GRCh38
NC_000003.11:g.194325132T>G , CM000665.1:g.194325132T>G	GRCh37
NC_000003.10:g.195806421T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1060A>C MANE Select	ENSP00000333355.6:p.Ser354Arg
ENST00000347147.8:c.1060A>C	ENSP00000333355.6:p.Ser354Arg
ENST00000381975.7:c.1056A>C	ENSP00000371402.3:p.Arg352=
ENST00000392432.6:c.1201A>C	ENSP00000376227.2:p.Ser401Arg
ENST00000419280.5:c.*356A>C	ENSP00000414077.1:n.*356A>C
ENST00000429560.1:c.252A>C	ENSP00000403053.1:p.Arg84=
ENST00000432352.5:c.334A>C	ENSP00000409963.1:p.Ser112Arg
ENST00000452358.5:c.559A>C	ENSP00000414333.1:p.Ser187Arg
ENST00000467284.1:n.106A>C
ENST00000473092.5:c.1060A>C	ENSP00000418674.1:p.Ser354Arg
ENST00000477651.5:n.824A>C
NM_001011655.2:c.1060A>C	NP_001011655.1:p.Ser354Arg
NM_001166305.1:c.1201A>C	NP_001159777.1:p.Ser401Arg
NM_001166306.1:c.1056A>C	NP_001159778.1:p.Arg352=
NM_138399.4:c.1060A>C	NP_612408.3:p.Ser354Arg
XM_005269371.3:c.1060A>C	XP_005269428.1:p.Ser354Arg
XM_011513318.1:c.1210A>C	XP_011511620.1:p.Ser404Arg
XM_011513319.1:c.1147A>C	XP_011511621.1:p.Ser383Arg
XM_011513320.1:c.1258A>C	XP_011511622.1:p.Ser420Arg
XM_011513321.1:c.1126A>C	XP_011511623.1:p.Ser376Arg
XM_011513322.1:c.1117A>C	XP_011511624.1:p.Ser373Arg
XM_011513323.1:c.955A>C	XP_011511625.1:p.Ser319Arg
XM_005269371.4:c.1060A>C	XP_005269428.1:p.Ser354Arg
XM_011513318.2:c.1210A>C	XP_011511620.1:p.Ser404Arg
XM_011513319.2:c.1147A>C	XP_011511621.1:p.Ser383Arg
XM_011513320.2:c.1258A>C	XP_011511622.1:p.Ser420Arg
XM_011513321.2:c.1126A>C	XP_011511623.1:p.Ser376Arg
XM_011513322.2:c.1117A>C	XP_011511624.1:p.Ser373Arg
XM_017007517.1:c.1069A>C	XP_016863006.1:p.Ser357Arg
XM_017007518.1:c.1069A>C	XP_016863007.1:p.Ser357Arg
NM_001011655.3:c.1060A>C MANE Select	NP_001011655.1:p.Ser354Arg
NM_001166305.2:c.1201A>C	NP_001159777.1:p.Ser401Arg
NM_001166306.2:c.1056A>C	NP_001159778.1:p.Arg352=
NM_138399.5:c.1060A>C	NP_612408.3:p.Ser354Arg