Canonical Allele Identifier: CA402373275

Gene: LOXHD1

Linked Data

• MyVariant Identifiers: chr18:g.44104747T>A (hg19) ; chr18:g.46524784T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46524784T>A , CM000680.2:g.46524784T>A	GRCh38
NC_000018.9:g.44104747T>A , CM000680.1:g.44104747T>A	GRCh37
NC_000018.8:g.42358745T>A	NCBI36
NG_016646.1:g.137250A>T
NG_016646.2:g.137250A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300591.11:c.1331A>T	ENSP00000300591.6:p.Glu444Val
ENST00000579038.6:c.1043A>T	ENSP00000463285.1:p.Glu348Val
ENST00000582408.6:c.1331A>T	ENSP00000461964.1:p.Glu444Val
ENST00000642948.1:c.4664A>T MANE Select	ENSP00000496347.1:p.Glu1555Val
ENST00000300591.10:c.1331A>T	ENSP00000300591.6:p.Glu444Val
ENST00000335730.6:n.3977A>T
ENST00000441551.6:c.4046A>T	ENSP00000387621.2:p.Glu1349Val
ENST00000536736.5:c.4664A>T	ENSP00000444586.1:p.Glu1555Val
ENST00000579038.5:c.1043A>T	ENSP00000463285.1:p.Glu348Val
ENST00000582408.5:c.1331A>T	ENSP00000461964.1:p.Glu444Val
NM_001145472.2:c.1331A>T	NP_001138944.1:p.Glu444Val
NM_001308013.1:c.1043A>T	NP_001294942.1:p.Glu348Val
NM_144612.6:c.4664A>T	NP_653213.6:p.Glu1555Val
XM_006722388.2:c.1463A>T	XP_006722451.1:p.Glu488Val
XM_006722389.2:c.1331A>T	XP_006722452.1:p.Glu444Val
XM_006722390.2:c.1331A>T	XP_006722453.1:p.Glu444Val
XM_006722391.2:c.1463A>T	XP_006722454.1:p.Glu488Val
XM_011525803.1:c.4664A>T	XP_011524105.1:p.Glu1555Val
XM_011525804.1:c.2825A>T	XP_011524106.1:p.Glu942Val
XM_011525805.1:c.1328A>T	XP_011524107.1:p.Glu443Val
XM_011525806.1:c.1043A>T	XP_011524108.1:p.Glu348Val
XM_011525807.1:c.1043A>T	XP_011524109.1:p.Glu348Val
XM_011525809.1:c.1043A>T	XP_011524111.1:p.Glu348Val
XM_006722388.3:c.1463A>T	XP_006722451.1:p.Glu488Val
XM_006722389.3:c.1331A>T	XP_006722452.1:p.Glu444Val
XM_006722390.3:c.1331A>T	XP_006722453.1:p.Glu444Val
XM_006722391.3:c.1463A>T	XP_006722454.1:p.Glu488Val
XM_011525804.2:c.2825A>T	XP_011524106.1:p.Glu942Val
XM_017025548.1:c.4046A>T	XP_016881037.1:p.Glu1349Val
XM_024451084.1:c.3146A>T	XP_024306852.1:p.Glu1049Val
XM_024451085.1:c.1328A>T	XP_024306853.1:p.Glu443Val
XM_024451086.1:c.1043A>T	XP_024306854.1:p.Glu348Val
XM_024451087.1:c.1043A>T	XP_024306855.1:p.Glu348Val
XM_024451088.1:c.1043A>T	XP_024306856.1:p.Glu348Val
NM_001145472.3:c.1331A>T	NP_001138944.1:p.Glu444Val
NM_001308013.2:c.1043A>T	NP_001294942.1:p.Glu348Val
NM_001384474.1:c.4664A>T MANE Select	NP_001371403.1:p.Glu1555Val
NM_144612.7:c.4664A>T	NP_653213.6:p.Glu1555Val