Canonical Allele Identifier: CA202114

Gene: LOXHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46534399G>C , CM000680.2:g.46534399G>C	GRCh38
NC_000018.9:g.44114362G>C , CM000680.1:g.44114362G>C	GRCh37
NC_000018.8:g.42368360G>C	NCBI36
NG_016646.1:g.127635C>G
NG_016646.2:g.127635C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001384474.1:c.4148C>G MANE Select	NP_001371403.1:p.Thr1383Arg
ENST00000642948.1:c.4148C>G MANE Select	ENSP00000496347.1:p.Thr1383Arg
NM_001145472.2:c.815C>G	NP_001138944.1:p.Thr272Arg
NM_001145472.3:c.815C>G	NP_001138944.1:p.Thr272Arg
NM_001308013.1:c.527C>G	NP_001294942.1:p.Thr176Arg
NM_001308013.2:c.527C>G	NP_001294942.1:p.Thr176Arg
NM_144612.6:c.4148C>G	NP_653213.6:p.Thr1383Arg
NM_144612.7:c.4148C>G	NP_653213.6:p.Thr1383Arg
ENST00000300591.10:c.815C>G	ENSP00000300591.6:p.Thr272Arg
ENST00000300591.11:c.815C>G	ENSP00000300591.6:p.Thr272Arg
ENST00000335730.6:n.3461C>G
ENST00000441551.6:c.3530C>G	ENSP00000387621.2:p.Thr1177Arg
ENST00000536111.1:c.854C>G	ENSP00000440060.1:p.Thr285Arg
ENST00000536736.5:c.4148C>G	ENSP00000444586.1:p.Thr1383Arg
ENST00000579038.5:c.527C>G	ENSP00000463285.1:p.Thr176Arg
ENST00000579038.6:c.527C>G	ENSP00000463285.1:p.Thr176Arg
ENST00000582408.5:c.815C>G	ENSP00000461964.1:p.Thr272Arg
ENST00000582408.6:c.815C>G	ENSP00000461964.1:p.Thr272Arg
XM_006722388.2:c.947C>G	XP_006722451.1:p.Thr316Arg
XM_006722388.3:c.947C>G	XP_006722451.1:p.Thr316Arg
XM_006722389.2:c.815C>G	XP_006722452.1:p.Thr272Arg
XM_006722389.3:c.815C>G	XP_006722452.1:p.Thr272Arg
XM_006722390.2:c.815C>G	XP_006722453.1:p.Thr272Arg
XM_006722390.3:c.815C>G	XP_006722453.1:p.Thr272Arg
XM_006722391.2:c.947C>G	XP_006722454.1:p.Thr316Arg
XM_006722391.3:c.947C>G	XP_006722454.1:p.Thr316Arg
XM_011525803.1:c.4148C>G	XP_011524105.1:p.Thr1383Arg
XM_011525804.1:c.2309C>G	XP_011524106.1:p.Thr770Arg
XM_011525804.2:c.2309C>G	XP_011524106.1:p.Thr770Arg
XM_011525805.1:c.812C>G	XP_011524107.1:p.Thr271Arg
XM_011525806.1:c.527C>G	XP_011524108.1:p.Thr176Arg
XM_011525807.1:c.527C>G	XP_011524109.1:p.Thr176Arg
XM_011525809.1:c.527C>G	XP_011524111.1:p.Thr176Arg
XM_017025548.1:c.3530C>G	XP_016881037.1:p.Thr1177Arg
XM_024451084.1:c.2630C>G	XP_024306852.1:p.Thr877Arg
XM_024451085.1:c.812C>G	XP_024306853.1:p.Thr271Arg
XM_024451086.1:c.527C>G	XP_024306854.1:p.Thr176Arg
XM_024451087.1:c.527C>G	XP_024306855.1:p.Thr176Arg
XM_024451088.1:c.527C>G	XP_024306856.1:p.Thr176Arg