Canonical Allele Identifier: CA2300898096

Gene: LOXHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46579648G= , CM000680.2:g.46579648G=	GRCh38
NC_000018.9:g.44159611G= , CM000680.1:g.44159611G=	GRCh37
NC_000018.8:g.42413609G=	NCBI36
NG_016646.1:g.82386C=
NG_016646.2:g.82386C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642948.1:c.1791C= MANE Select	ENSP00000496347.1:p.Asp597=
ENST00000335730.6:n.1104C=
ENST00000441551.6:c.1791C=	ENSP00000387621.2:p.Asp597=
ENST00000536736.5:c.1791C=	ENSP00000444586.1:p.Asp597=
NM_144612.6:c.1791C=	NP_653213.6:p.Asp597=
XM_011525803.1:c.1791C=	XP_011524105.1:p.Asp597=
XM_011525804.1:c.-30-1781C=	XP_011524106.1:n.-30-1781C=
XM_011525804.2:c.-30-1781C=	XP_011524106.1:n.-30-1781C=
XM_017025548.1:c.1791C=	XP_016881037.1:p.Asp597=
XM_024451084.1:c.273C=	XP_024306852.1:p.Asp91=
NM_001384474.1:c.1791C= MANE Select	NP_001371403.1:p.Asp597=
NM_144612.7:c.1791C=	NP_653213.6:p.Asp597=