Canonical Allele Identifier: CA2300898065

Gene: LOXHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46579597_46579598delinsAG , CM000680.2:g.46579597_46579598delinsAG	GRCh38
NC_000018.9:g.44159560_44159561delinsAG , CM000680.1:g.44159560_44159561delinsAG	GRCh37
NC_000018.8:g.42413558_42413559delinsAG	NCBI36
NG_016646.1:g.82436_82437delinsCT
NG_016646.2:g.82436_82437delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000642948.1:c.1809+32_1809+33delinsCT MANE Select	ENSP00000496347.1:n.1809+32_1809+33delins...
ENST00000335730.6:n.1122+32_1122+33delinsCT
ENST00000441551.6:c.1809+32_1809+33delinsCT	ENSP00000387621.2:n.1809+32_1809+33delins...
ENST00000536736.5:c.1809+32_1809+33delinsCT	ENSP00000444586.1:n.1809+32_1809+33delins...
NM_144612.6:c.1809+32_1809+33delinsCT	NP_653213.6:n.1809+32_1809+33delinsCT
XM_011525803.1:c.1809+32_1809+33delinsCT	XP_011524105.1:n.1809+32_1809+33delinsCT
XM_011525804.1:c.-30-1731_-30-1730delinsCT	XP_011524106.1:n.-30-1731_-30-1730delinsC...
XM_011525804.2:c.-30-1731_-30-1730delinsCT	XP_011524106.1:n.-30-1731_-30-1730delinsC...
XM_017025548.1:c.1809+32_1809+33delinsCT	XP_016881037.1:n.1809+32_1809+33delinsCT
XM_024451084.1:c.291+32_291+33delinsCT	XP_024306852.1:n.291+32_291+33delinsCT
NM_001384474.1:c.1809+32_1809+33delinsCT MANE Select	NP_001371403.1:n.1809+32_1809+33delinsCT
NM_144612.7:c.1809+32_1809+33delinsCT	NP_653213.6:n.1809+32_1809+33delinsCT