Canonical Allele Identifier: CA402366854

Gene: LOXHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46489130C>A , CM000680.2:g.46489130C>A	GRCh38
NC_000018.9:g.44069093C>A , CM000680.1:g.44069093C>A	GRCh37
NC_000018.8:g.42323091C>A	NCBI36
NG_016646.1:g.172904G>T
NG_016646.2:g.172904G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300591.11:c.2558G>T	ENSP00000300591.6:p.Gly853Val
ENST00000398705.7:c.608G>T	ENSP00000381692.2:p.Gly203Val
ENST00000579038.6:c.2270G>T	ENSP00000463285.1:p.Gly757Val
ENST00000582408.6:c.2372G>T	ENSP00000461964.1:p.Gly791Val
ENST00000642948.1:c.5891G>T MANE Select	ENSP00000496347.1:p.Gly1964Val
ENST00000300591.10:c.2558G>T	ENSP00000300591.6:p.Gly853Val
ENST00000398686.8:c.608G>T	ENSP00000381676.4:p.Gly203Val
ENST00000398705.6:c.608G>T	ENSP00000381692.2:p.Gly203Val
ENST00000441551.6:c.5273G>T	ENSP00000387621.2:p.Gly1758Val
ENST00000536736.5:c.5705G>T	ENSP00000444586.1:p.Gly1902Val
ENST00000579038.5:c.2270G>T	ENSP00000463285.1:p.Gly757Val
ENST00000582408.5:c.2372G>T	ENSP00000461964.1:p.Gly791Val
NM_001145472.2:c.2558G>T	NP_001138944.1:p.Gly853Val
NM_001145473.2:c.608G>T	NP_001138945.1:p.Gly203Val
NM_001173129.1:c.608G>T	NP_001166600.1:p.Gly203Val
NM_001308013.1:c.2270G>T	NP_001294942.1:p.Gly757Val
NM_144612.6:c.5705G>T	NP_653213.6:p.Gly1902Val
XM_006722388.2:c.2690G>T	XP_006722451.1:p.Gly897Val
XM_006722389.2:c.2558G>T	XP_006722452.1:p.Gly853Val
XM_006722390.2:c.2558G>T	XP_006722453.1:p.Gly853Val
XM_006722391.2:c.2504G>T	XP_006722454.1:p.Gly835Val
XM_011525803.1:c.5891G>T	XP_011524105.1:p.Gly1964Val
XM_011525804.1:c.4052G>T	XP_011524106.1:p.Gly1351Val
XM_011525805.1:c.2555G>T	XP_011524107.1:p.Gly852Val
XM_011525806.1:c.2270G>T	XP_011524108.1:p.Gly757Val
XM_011525807.1:c.2270G>T	XP_011524109.1:p.Gly757Val
XM_011525809.1:c.2270G>T	XP_011524111.1:p.Gly757Val
XM_011525810.1:c.659G>T	XP_011524112.1:p.Gly220Val
XM_011525811.1:c.608G>T	XP_011524113.1:p.Gly203Val
XM_006722388.3:c.2690G>T	XP_006722451.1:p.Gly897Val
XM_006722389.3:c.2558G>T	XP_006722452.1:p.Gly853Val
XM_006722390.3:c.2558G>T	XP_006722453.1:p.Gly853Val
XM_006722391.3:c.2504G>T	XP_006722454.1:p.Gly835Val
XM_011525804.2:c.4052G>T	XP_011524106.1:p.Gly1351Val
XM_011525810.2:c.659G>T	XP_011524112.1:p.Gly220Val
XM_011525811.2:c.608G>T	XP_011524113.1:p.Gly203Val
XM_017025548.1:c.5273G>T	XP_016881037.1:p.Gly1758Val
XM_024451084.1:c.4373G>T	XP_024306852.1:p.Gly1458Val
XM_024451085.1:c.2555G>T	XP_024306853.1:p.Gly852Val
XM_024451086.1:c.2270G>T	XP_024306854.1:p.Gly757Val
XM_024451087.1:c.2270G>T	XP_024306855.1:p.Gly757Val
XM_024451088.1:c.2270G>T	XP_024306856.1:p.Gly757Val
NM_001145472.3:c.2558G>T	NP_001138944.1:p.Gly853Val
NM_001145473.3:c.608G>T	NP_001138945.1:p.Gly203Val
NM_001173129.2:c.608G>T	NP_001166600.1:p.Gly203Val
NM_001308013.2:c.2270G>T	NP_001294942.1:p.Gly757Val
NM_001384474.1:c.5891G>T MANE Select	NP_001371403.1:p.Gly1964Val
NM_144612.7:c.5705G>T	NP_653213.6:p.Gly1902Val