Canonical Allele Identifier: CA2300898024

Gene: LOXHD1

Linked Data

• dbSNP Id: rs2037921755

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46579524_46579525insTGGGG , CM000680.2:g.46579524_46579525insTGGGG	GRCh38
NC_000018.9:g.44159487_44159488insTGGGG , CM000680.1:g.44159487_44159488insTGGGG	GRCh37
NC_000018.8:g.42413485_42413486insTGGGG	NCBI36
NG_016646.1:g.82509_82510insCCCCA
NG_016646.2:g.82509_82510insCCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642948.1:c.1809+105_1809+106insCCCCA MANE Select	ENSP00000496347.1:n.1809+105_1809+106insCCCCA
ENST00000335730.6:n.1122+105_1122+106insCCCCA
ENST00000441551.6:c.1809+105_1809+106insCCCCA	ENSP00000387621.2:n.1809+105_1809+106insCCCCA
ENST00000536736.5:c.1809+105_1809+106insCCCCA	ENSP00000444586.1:n.1809+105_1809+106insCCCCA
NM_144612.6:c.1809+105_1809+106insCCCCA	NP_653213.6:n.1809+105_1809+106insCCCCA
XM_011525803.1:c.1809+105_1809+106insCCCCA	XP_011524105.1:n.1809+105_1809+106insCCCCA
XM_011525804.1:c.-30-1658_-30-1657insCCCCA	XP_011524106.1:n.-30-1658_-30-1657insCCCCA
XM_011525804.2:c.-30-1658_-30-1657insCCCCA	XP_011524106.1:n.-30-1658_-30-1657insCCCCA
XM_017025548.1:c.1809+105_1809+106insCCCCA	XP_016881037.1:n.1809+105_1809+106insCCCCA
XM_024451084.1:c.291+105_291+106insCCCCA	XP_024306852.1:n.291+105_291+106insCCCCA
NM_001384474.1:c.1809+105_1809+106insCCCCA MANE Select	NP_001371403.1:n.1809+105_1809+106insCCCCA
NM_144612.7:c.1809+105_1809+106insCCCCA	NP_653213.6:n.1809+105_1809+106insCCCCA