Canonical Allele Identifier: CA2300894586
Gene: LOXHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46572128C= , CM000680.2:g.46572128C= GRCh38
NC_000018.9:g.44152091C= , CM000680.1:g.44152091C= GRCh37
NC_000018.8:g.42406089C= NCBI36
NG_016646.1:g.89906G=
NG_016646.2:g.89906G=

Transcript Alleles

HGVS Amino-acid change
ENST00000642948.1:c.2005G= MANE Select ENSP00000496347.1:p.Val669=
ENST00000335730.6:n.1318G=
ENST00000441551.6:c.2005G= ENSP00000387621.2:p.Val669=
ENST00000536736.5:c.2005G= ENSP00000444586.1:p.Val669=
NM_144612.6:c.2005G= NP_653213.6:p.Val669=
XM_011525803.1:c.2005G= XP_011524105.1:p.Val669=
XM_011525804.1:c.166G= XP_011524106.1:p.Val56=
XM_011525804.2:c.166G= XP_011524106.1:p.Val56=
XM_017025548.1:c.2005G= XP_016881037.1:p.Val669=
XM_024451084.1:c.487G= XP_024306852.1:p.Val163=
NM_001384474.1:c.2005G= MANE Select NP_001371403.1:p.Val669=
NM_144612.7:c.2005G= NP_653213.6:p.Val669=