Canonical Allele Identifier: CA2300894544
Gene: LOXHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46572048A= , CM000680.2:g.46572048A= GRCh38
NC_000018.9:g.44152011A= , CM000680.1:g.44152011A= GRCh37
NC_000018.8:g.42406009A= NCBI36
NG_016646.1:g.89986T=
NG_016646.2:g.89986T=

Transcript Alleles

HGVS Amino-acid change
ENST00000642948.1:c.2047+38T= MANE Select ENSP00000496347.1:n.2047+38T=
ENST00000335730.6:n.1360+38T=
ENST00000441551.6:c.2047+38T= ENSP00000387621.2:n.2047+38T=
ENST00000536736.5:c.2047+38T= ENSP00000444586.1:n.2047+38T=
NM_144612.6:c.2047+38T= NP_653213.6:n.2047+38T=
XM_011525803.1:c.2047+38T= XP_011524105.1:n.2047+38T=
XM_011525804.1:c.208+38T= XP_011524106.1:n.208+38T=
XM_011525804.2:c.208+38T= XP_011524106.1:n.208+38T=
XM_017025548.1:c.2047+38T= XP_016881037.1:n.2047+38T=
XM_024451084.1:c.529+38T= XP_024306852.1:n.529+38T=
NM_001384474.1:c.2047+38T= MANE Select NP_001371403.1:n.2047+38T=
NM_144612.7:c.2047+38T= NP_653213.6:n.2047+38T=