Canonical Allele Identifier: CA7640022

Gene: THSD4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71765188G>A , CM000677.2:g.71765188G>A	GRCh38
NC_000015.9:g.72057527G>A , CM000677.1:g.72057527G>A	GRCh37
NC_000015.8:g.69844581G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024817.3:c.2758G>A MANE Select	NP_079093.2:p.Glu920Lys
ENST00000261862.8:c.2758G>A MANE Select	ENSP00000261862.8:p.Glu920Lys
NM_001286429.1:c.1678G>A	NP_001273358.1:p.Glu560Lys
NM_001286429.2:c.1678G>A	NP_001273358.1:p.Glu560Lys
NM_001394532.1:c.2758G>A	NP_001381461.1:p.Glu920Lys
NM_024817.2:c.2758G>A	NP_079093.2:p.Glu920Lys
ENST00000261862.7:c.270-15354G>A	ENSP00000261862.7:n.270-15354G>A
ENST00000355327.7:c.2758G>A	ENSP00000347484.3:p.Glu920Lys
ENST00000357769.4:c.1678G>A	ENSP00000350413.4:p.Glu560Lys
ENST00000567838.1:n.1681G>A
XM_006720692.2:c.2758G>A	XP_006720755.1:p.Glu920Lys
XM_006720692.3:c.2758G>A	XP_006720755.1:p.Glu920Lys
XM_011522043.1:c.1792G>A	XP_011520345.1:p.Glu598Lys
XM_011522043.3:c.1792G>A	XP_011520345.1:p.Glu598Lys
XM_011522044.1:c.1750G>A	XP_011520346.1:p.Glu584Lys
XM_011522044.2:c.1750G>A	XP_011520346.1:p.Glu584Lys
XM_011522045.1:c.1624G>A	XP_011520347.1:p.Glu542Lys
XM_017022582.2:c.1876G>A	XP_016878071.1:p.Glu626Lys
XM_017022583.1:c.1780G>A	XP_016878072.1:p.Glu594Lys
XM_017022584.1:c.1732G>A	XP_016878073.1:p.Glu578Lys
XM_017022585.1:c.1726G>A	XP_016878074.1:p.Glu576Lys
XM_017022586.1:c.1705G>A	XP_016878075.1:p.Glu569Lys