Canonical Allele Identifier: CA355825032

Gene: TMEM44

Linked Data

• MyVariant Identifiers: chr3:g.194325143T>A (hg19) ; chr3:g.194604414T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604414T>A , CM000665.2:g.194604414T>A	GRCh38
NC_000003.11:g.194325143T>A , CM000665.1:g.194325143T>A	GRCh37
NC_000003.10:g.195806432T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1049A>T MANE Select	ENSP00000333355.6:p.Asp350Val
ENST00000347147.8:c.1049A>T	ENSP00000333355.6:p.Asp350Val
ENST00000381975.7:c.1045A>T	ENSP00000371402.3:p.Thr349Ser
ENST00000392432.6:c.1190A>T	ENSP00000376227.2:p.Asp397Val
ENST00000419280.5:c.*345A>T	ENSP00000414077.1:n.*345A>T
ENST00000429560.1:c.241A>T	ENSP00000403053.1:p.Thr81Ser
ENST00000432352.5:c.323A>T	ENSP00000409963.1:p.Asp108Val
ENST00000452358.5:c.548A>T	ENSP00000414333.1:p.Asp183Val
ENST00000467284.1:n.95A>T
ENST00000473092.5:c.1049A>T	ENSP00000418674.1:p.Asp350Val
ENST00000477651.5:n.813A>T
NM_001011655.2:c.1049A>T	NP_001011655.1:p.Asp350Val
NM_001166305.1:c.1190A>T	NP_001159777.1:p.Asp397Val
NM_001166306.1:c.1045A>T	NP_001159778.1:p.Thr349Ser
NM_138399.4:c.1049A>T	NP_612408.3:p.Asp350Val
XM_005269371.3:c.1049A>T	XP_005269428.1:p.Asp350Val
XM_011513318.1:c.1199A>T	XP_011511620.1:p.Asp400Val
XM_011513319.1:c.1136A>T	XP_011511621.1:p.Asp379Val
XM_011513320.1:c.1247A>T	XP_011511622.1:p.Asp416Val
XM_011513321.1:c.1115A>T	XP_011511623.1:p.Asp372Val
XM_011513322.1:c.1106A>T	XP_011511624.1:p.Asp369Val
XM_011513323.1:c.944A>T	XP_011511625.1:p.Asp315Val
XM_005269371.4:c.1049A>T	XP_005269428.1:p.Asp350Val
XM_011513318.2:c.1199A>T	XP_011511620.1:p.Asp400Val
XM_011513319.2:c.1136A>T	XP_011511621.1:p.Asp379Val
XM_011513320.2:c.1247A>T	XP_011511622.1:p.Asp416Val
XM_011513321.2:c.1115A>T	XP_011511623.1:p.Asp372Val
XM_011513322.2:c.1106A>T	XP_011511624.1:p.Asp369Val
XM_017007517.1:c.1058A>T	XP_016863006.1:p.Asp353Val
XM_017007518.1:c.1058A>T	XP_016863007.1:p.Asp353Val
NM_001011655.3:c.1049A>T MANE Select	NP_001011655.1:p.Asp350Val
NM_001166305.2:c.1190A>T	NP_001159777.1:p.Asp397Val
NM_001166306.2:c.1045A>T	NP_001159778.1:p.Thr349Ser
NM_138399.5:c.1049A>T	NP_612408.3:p.Asp350Val