Canonical Allele Identifier: CA2300898026

Gene: LOXHD1

Linked Data

• dbSNP Id: rs2037921809

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46579526_46579527insAT , CM000680.2:g.46579526_46579527insAT	GRCh38
NC_000018.9:g.44159489_44159490insAT , CM000680.1:g.44159489_44159490insAT	GRCh37
NC_000018.8:g.42413487_42413488insAT	NCBI36
NG_016646.1:g.82507_82508insAT
NG_016646.2:g.82507_82508insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642948.1:c.1809+103_1809+104insAT MANE Select	ENSP00000496347.1:n.1809+103_1809+104insAT
ENST00000335730.6:n.1122+103_1122+104insAT
ENST00000441551.6:c.1809+103_1809+104insAT	ENSP00000387621.2:n.1809+103_1809+104insAT
ENST00000536736.5:c.1809+103_1809+104insAT	ENSP00000444586.1:n.1809+103_1809+104insAT
NM_144612.6:c.1809+103_1809+104insAT	NP_653213.6:n.1809+103_1809+104insAT
XM_011525803.1:c.1809+103_1809+104insAT	XP_011524105.1:n.1809+103_1809+104insAT
XM_011525804.1:c.-30-1660_-30-1659insAT	XP_011524106.1:n.-30-1660_-30-1659insAT
XM_011525804.2:c.-30-1660_-30-1659insAT	XP_011524106.1:n.-30-1660_-30-1659insAT
XM_017025548.1:c.1809+103_1809+104insAT	XP_016881037.1:n.1809+103_1809+104insAT
XM_024451084.1:c.291+103_291+104insAT	XP_024306852.1:n.291+103_291+104insAT
NM_001384474.1:c.1809+103_1809+104insAT MANE Select	NP_001371403.1:n.1809+103_1809+104insAT
NM_144612.7:c.1809+103_1809+104insAT	NP_653213.6:n.1809+103_1809+104insAT