Canonical Allele Identifier: CA2300898116
Gene: LOXHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46579686C= , CM000680.2:g.46579686C= GRCh38
NC_000018.9:g.44159649C= , CM000680.1:g.44159649C= GRCh37
NC_000018.8:g.42413647C= NCBI36
NG_016646.1:g.82348G=
NG_016646.2:g.82348G=

Transcript Alleles

HGVS Amino-acid change
ENST00000642948.1:c.1753G= MANE Select ENSP00000496347.1:p.Gly585=
ENST00000335730.6:n.1066G=
ENST00000441551.6:c.1753G= ENSP00000387621.2:p.Gly585=
ENST00000536736.5:c.1753G= ENSP00000444586.1:p.Gly585=
NM_144612.6:c.1753G= NP_653213.6:p.Gly585=
XM_011525803.1:c.1753G= XP_011524105.1:p.Gly585=
XM_011525804.1:c.-30-1819G= XP_011524106.1:n.-30-1819G=
XM_011525804.2:c.-30-1819G= XP_011524106.1:n.-30-1819G=
XM_017025548.1:c.1753G= XP_016881037.1:p.Gly585=
XM_024451084.1:c.235G= XP_024306852.1:p.Gly79=
NM_001384474.1:c.1753G= MANE Select NP_001371403.1:p.Gly585=
NM_144612.7:c.1753G= NP_653213.6:p.Gly585=