Canonical Allele Identifier: CA2300898246

Gene: LOXHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46579962_46579963delinsTC , CM000680.2:g.46579962_46579963delinsTC	GRCh38
NC_000018.9:g.44159925_44159926delinsTC , CM000680.1:g.44159925_44159926delinsTC	GRCh37
NC_000018.8:g.42413923_42413924delinsTC	NCBI36
NG_016646.1:g.82071_82072delinsGA
NG_016646.2:g.82071_82072delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642948.1:c.1655-179_1655-178delinsGA MANE Select	ENSP00000496347.1:n.1655-179_1655-178delinsGA
ENST00000335730.6:n.968-179_968-178delinsGA
ENST00000441551.6:c.1655-179_1655-178delinsGA	ENSP00000387621.2:n.1655-179_1655-178delinsGA
ENST00000536736.5:c.1655-179_1655-178delinsGA	ENSP00000444586.1:n.1655-179_1655-178delinsGA
NM_144612.6:c.1655-179_1655-178delinsGA	NP_653213.6:n.1655-179_1655-178delinsGA
XM_011525803.1:c.1655-179_1655-178delinsGA	XP_011524105.1:n.1655-179_1655-178delinsGA
XM_011525804.1:c.-30-2096_-30-2095delinsGA	XP_011524106.1:n.-30-2096_-30-2095delinsGA
XM_011525804.2:c.-30-2096_-30-2095delinsGA	XP_011524106.1:n.-30-2096_-30-2095delinsGA
XM_017025548.1:c.1655-179_1655-178delinsGA	XP_016881037.1:n.1655-179_1655-178delinsGA
XM_024451084.1:c.137-179_137-178delinsGA	XP_024306852.1:n.137-179_137-178delinsGA
NM_001384474.1:c.1655-179_1655-178delinsGA MANE Select	NP_001371403.1:n.1655-179_1655-178delinsGA
NM_144612.7:c.1655-179_1655-178delinsGA	NP_653213.6:n.1655-179_1655-178delinsGA