Canonical Allele Identifier: CA355824872

Gene: TMEM44

Linked Data

• MyVariant Identifiers: chr3:g.194325082C>T (hg19) ; chr3:g.194604353C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604353C>T , CM000665.2:g.194604353C>T	GRCh38
NC_000003.11:g.194325082C>T , CM000665.1:g.194325082C>T	GRCh37
NC_000003.10:g.195806371C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1110G>A MANE Select	ENSP00000333355.6:p.Gln370=
ENST00000347147.8:c.1110G>A	ENSP00000333355.6:p.Gln370=
ENST00000381975.7:c.1106G>A	ENSP00000371402.3:p.Arg369Lys
ENST00000392432.6:c.1251G>A	ENSP00000376227.2:p.Gln417=
ENST00000419280.5:c.*406G>A	ENSP00000414077.1:n.*406G>A
ENST00000429560.1:c.302G>A	ENSP00000403053.1:p.Arg101Lys
ENST00000432352.5:c.384G>A	ENSP00000409963.1:p.Gln128=
ENST00000452358.5:c.609G>A	ENSP00000414333.1:p.Gln203=
ENST00000467284.1:n.156G>A
ENST00000473092.5:c.1110G>A	ENSP00000418674.1:p.Gln370=
ENST00000477651.5:n.874G>A
NM_001011655.2:c.1110G>A	NP_001011655.1:p.Gln370=
NM_001166305.1:c.1251G>A	NP_001159777.1:p.Gln417=
NM_001166306.1:c.1106G>A	NP_001159778.1:p.Arg369Lys
NM_138399.4:c.1110G>A	NP_612408.3:p.Gln370=
XM_005269371.3:c.1110G>A	XP_005269428.1:p.Gln370=
XM_011513318.1:c.1260G>A	XP_011511620.1:p.Gln420=
XM_011513319.1:c.1197G>A	XP_011511621.1:p.Gln399=
XM_011513320.1:c.1308G>A	XP_011511622.1:p.Gln436=
XM_011513321.1:c.1176G>A	XP_011511623.1:p.Gln392=
XM_011513322.1:c.1167G>A	XP_011511624.1:p.Gln389=
XM_011513323.1:c.1005G>A	XP_011511625.1:p.Gln335=
XM_005269371.4:c.1110G>A	XP_005269428.1:p.Gln370=
XM_011513318.2:c.1260G>A	XP_011511620.1:p.Gln420=
XM_011513319.2:c.1197G>A	XP_011511621.1:p.Gln399=
XM_011513320.2:c.1308G>A	XP_011511622.1:p.Gln436=
XM_011513321.2:c.1176G>A	XP_011511623.1:p.Gln392=
XM_011513322.2:c.1167G>A	XP_011511624.1:p.Gln389=
XM_017007517.1:c.1119G>A	XP_016863006.1:p.Gln373=
XM_017007518.1:c.1119G>A	XP_016863007.1:p.Gln373=
NM_001011655.3:c.1110G>A MANE Select	NP_001011655.1:p.Gln370=
NM_001166305.2:c.1251G>A	NP_001159777.1:p.Gln417=
NM_001166306.2:c.1106G>A	NP_001159778.1:p.Arg369Lys
NM_138399.5:c.1110G>A	NP_612408.3:p.Gln370=