Canonical Allele Identifier: CA2300898113
Gene: LOXHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46579682T= , CM000680.2:g.46579682T= GRCh38
NC_000018.9:g.44159645T= , CM000680.1:g.44159645T= GRCh37
NC_000018.8:g.42413643T= NCBI36
NG_016646.1:g.82352A=
NG_016646.2:g.82352A=

Transcript Alleles

HGVS Amino-acid change
ENST00000642948.1:c.1757A= MANE Select ENSP00000496347.1:p.Glu586=
ENST00000335730.6:n.1070A=
ENST00000441551.6:c.1757A= ENSP00000387621.2:p.Glu586=
ENST00000536736.5:c.1757A= ENSP00000444586.1:p.Glu586=
NM_144612.6:c.1757A= NP_653213.6:p.Glu586=
XM_011525803.1:c.1757A= XP_011524105.1:p.Glu586=
XM_011525804.1:c.-30-1815A= XP_011524106.1:n.-30-1815A=
XM_011525804.2:c.-30-1815A= XP_011524106.1:n.-30-1815A=
XM_017025548.1:c.1757A= XP_016881037.1:p.Glu586=
XM_024451084.1:c.239A= XP_024306852.1:p.Glu80=
NM_001384474.1:c.1757A= MANE Select NP_001371403.1:p.Glu586=
NM_144612.7:c.1757A= NP_653213.6:p.Glu586=