Canonical Allele Identifier: CA2300898123

Gene: LOXHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46579697A= , CM000680.2:g.46579697A=	GRCh38
NC_000018.9:g.44159660A= , CM000680.1:g.44159660A=	GRCh37
NC_000018.8:g.42413658A=	NCBI36
NG_016646.1:g.82337T=
NG_016646.2:g.82337T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642948.1:c.1742T= MANE Select	ENSP00000496347.1:p.Val581=
ENST00000335730.6:n.1055T=
ENST00000441551.6:c.1742T=	ENSP00000387621.2:p.Val581=
ENST00000536736.5:c.1742T=	ENSP00000444586.1:p.Val581=
NM_144612.6:c.1742T=	NP_653213.6:p.Val581=
XM_011525803.1:c.1742T=	XP_011524105.1:p.Val581=
XM_011525804.1:c.-30-1830T=	XP_011524106.1:n.-30-1830T=
XM_011525804.2:c.-30-1830T=	XP_011524106.1:n.-30-1830T=
XM_017025548.1:c.1742T=	XP_016881037.1:p.Val581=
XM_024451084.1:c.224T=	XP_024306852.1:p.Val75=
NM_001384474.1:c.1742T= MANE Select	NP_001371403.1:p.Val581=
NM_144612.7:c.1742T=	NP_653213.6:p.Val581=