Canonical Allele Identifier: CA2300894484

Gene: LOXHD1

Linked Data

• dbSNP Id: rs435770

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46571932T>A , CM000680.2:g.46571932T>A	GRCh38
NC_000018.9:g.44151895T>A , CM000680.1:g.44151895T>A	GRCh37
NC_000018.8:g.42405893T>A	NCBI36
NG_016646.1:g.90102A>T
NG_016646.2:g.90102A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642948.1:c.2047+154A>T MANE Select	ENSP00000496347.1:n.2047+154A>T
ENST00000335730.6:n.1360+154A>T
ENST00000441551.6:c.2047+154A>T	ENSP00000387621.2:n.2047+154A>T
ENST00000536736.5:c.2047+154A>T	ENSP00000444586.1:n.2047+154A>T
NM_144612.6:c.2047+154A>T	NP_653213.6:n.2047+154A>T
XM_011525803.1:c.2047+154A>T	XP_011524105.1:n.2047+154A>T
XM_011525804.1:c.208+154A>T	XP_011524106.1:n.208+154A>T
XM_011525804.2:c.208+154A>T	XP_011524106.1:n.208+154A>T
XM_017025548.1:c.2047+154A>T	XP_016881037.1:n.2047+154A>T
XM_024451084.1:c.529+154A>T	XP_024306852.1:n.529+154A>T
NM_001384474.1:c.2047+154A>T MANE Select	NP_001371403.1:n.2047+154A>T
NM_144612.7:c.2047+154A>T	NP_653213.6:n.2047+154A>T