Canonical Allele Identifier: CA2300872219
Gene: LOXHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46524773G= , CM000680.2:g.46524773G= GRCh38
NC_000018.9:g.44104736G= , CM000680.1:g.44104736G= GRCh37
NC_000018.8:g.42358734G= NCBI36
NG_016646.1:g.137261C=
NG_016646.2:g.137261C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300591.11:c.1342C= ENSP00000300591.6:p.Leu448=
ENST00000579038.6:c.1054C= ENSP00000463285.1:p.Leu352=
ENST00000582408.6:c.1342C= ENSP00000461964.1:p.Leu448=
ENST00000642948.1:c.4675C= MANE Select ENSP00000496347.1:p.Leu1559=
ENST00000300591.10:c.1342C= ENSP00000300591.6:p.Leu448=
ENST00000335730.6:n.3988C=
ENST00000441551.6:c.4057C= ENSP00000387621.2:p.Leu1353=
ENST00000536736.5:c.4675C= ENSP00000444586.1:p.Leu1559=
ENST00000579038.5:c.1054C= ENSP00000463285.1:p.Leu352=
ENST00000582408.5:c.1342C= ENSP00000461964.1:p.Leu448=
NM_001145472.2:c.1342C= NP_001138944.1:p.Leu448=
NM_001308013.1:c.1054C= NP_001294942.1:p.Leu352=
NM_144612.6:c.4675C= NP_653213.6:p.Leu1559=
XM_006722388.2:c.1474C= XP_006722451.1:p.Leu492=
XM_006722389.2:c.1342C= XP_006722452.1:p.Leu448=
XM_006722390.2:c.1342C= XP_006722453.1:p.Leu448=
XM_006722391.2:c.1474C= XP_006722454.1:p.Leu492=
XM_011525803.1:c.4675C= XP_011524105.1:p.Leu1559=
XM_011525804.1:c.2836C= XP_011524106.1:p.Leu946=
XM_011525805.1:c.1339C= XP_011524107.1:p.Leu447=
XM_011525806.1:c.1054C= XP_011524108.1:p.Leu352=
XM_011525807.1:c.1054C= XP_011524109.1:p.Leu352=
XM_011525809.1:c.1054C= XP_011524111.1:p.Leu352=
XM_006722388.3:c.1474C= XP_006722451.1:p.Leu492=
XM_006722389.3:c.1342C= XP_006722452.1:p.Leu448=
XM_006722390.3:c.1342C= XP_006722453.1:p.Leu448=
XM_006722391.3:c.1474C= XP_006722454.1:p.Leu492=
XM_011525804.2:c.2836C= XP_011524106.1:p.Leu946=
XM_017025548.1:c.4057C= XP_016881037.1:p.Leu1353=
XM_024451084.1:c.3157C= XP_024306852.1:p.Leu1053=
XM_024451085.1:c.1339C= XP_024306853.1:p.Leu447=
XM_024451086.1:c.1054C= XP_024306854.1:p.Leu352=
XM_024451087.1:c.1054C= XP_024306855.1:p.Leu352=
XM_024451088.1:c.1054C= XP_024306856.1:p.Leu352=
NM_001145472.3:c.1342C= NP_001138944.1:p.Leu448=
NM_001308013.2:c.1054C= NP_001294942.1:p.Leu352=
NM_001384474.1:c.4675C= MANE Select NP_001371403.1:p.Leu1559=
NM_144612.7:c.4675C= NP_653213.6:p.Leu1559=