Canonical Allele Identifier: CA919978894

Gene: LOXHD1

Linked Data

• dbSNP Id: rs1599023909
• gnomAD v4: 18-46579906-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46579911del , CM000680.2:g.46579911del	GRCh38
NC_000018.9:g.44159874del , CM000680.1:g.44159874del	GRCh37
NC_000018.8:g.42413872del	NCBI36
NG_016646.1:g.82127del
NG_016646.2:g.82127del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642948.1:c.1655-123del MANE Select	ENSP00000496347.1:n.1655-123del
ENST00000335730.6:n.968-123del
ENST00000441551.6:c.1655-123del	ENSP00000387621.2:n.1655-123del
ENST00000536736.5:c.1655-123del	ENSP00000444586.1:n.1655-123del
NM_144612.6:c.1655-123del	NP_653213.6:n.1655-123del
XM_011525803.1:c.1655-123del	XP_011524105.1:n.1655-123del
XM_011525804.1:c.-30-2040del	XP_011524106.1:n.-30-2040del
XM_011525804.2:c.-30-2040del	XP_011524106.1:n.-30-2040del
XM_017025548.1:c.1655-123del	XP_016881037.1:n.1655-123del
XM_024451084.1:c.137-123del	XP_024306852.1:n.137-123del
NM_001384474.1:c.1655-123del MANE Select	NP_001371403.1:n.1655-123del
NM_144612.7:c.1655-123del	NP_653213.6:n.1655-123del