Canonical Allele Identifier: CA2300890559

Gene: LOXHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46563166G= , CM000680.2:g.46563166G=	GRCh38
NC_000018.9:g.44143129G= , CM000680.1:g.44143129G=	GRCh37
NC_000018.8:g.42397127G=	NCBI36
NG_016646.1:g.98868C=
NG_016646.2:g.98868C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001384474.1:c.2497C= MANE Select	NP_001371403.1:p.Arg833=
ENST00000642948.1:c.2497C= MANE Select	ENSP00000496347.1:p.Arg833=
NM_144612.6:c.2497C=	NP_653213.6:p.Arg833=
NM_144612.7:c.2497C=	NP_653213.6:p.Arg833=
ENST00000335730.6:n.1810C=
ENST00000441551.6:c.2497C=	ENSP00000387621.2:p.Arg833=
ENST00000536736.5:c.2497C=	ENSP00000444586.1:p.Arg833=
XM_011525803.1:c.2497C=	XP_011524105.1:p.Arg833=
XM_011525804.1:c.658C=	XP_011524106.1:p.Arg220=
XM_011525804.2:c.658C=	XP_011524106.1:p.Arg220=
XM_017025548.1:c.2497C=	XP_016881037.1:p.Arg833=
XM_024451084.1:c.979C=	XP_024306852.1:p.Arg327=