Canonical Allele Identifier: CA8952602

Gene: LOXHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46560273C>T , CM000680.2:g.46560273C>T	GRCh38
NC_000018.9:g.44140236C>T , CM000680.1:g.44140236C>T	GRCh37
NC_000018.8:g.42394234C>T	NCBI36
NG_016646.1:g.101761G>A
NG_016646.2:g.101761G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642948.1:c.2871G>A MANE Select	ENSP00000496347.1:p.Ser957=
ENST00000335730.6:n.2184G>A
ENST00000441551.6:c.2599-2784G>A	ENSP00000387621.2:n.2599-2784G>A
ENST00000536736.5:c.2871G>A	ENSP00000444586.1:p.Ser957=
NM_144612.6:c.2871G>A	NP_653213.6:p.Ser957=
XM_011525803.1:c.2871G>A	XP_011524105.1:p.Ser957=
XM_011525804.1:c.1032G>A	XP_011524106.1:p.Ser344=
XM_011525804.2:c.1032G>A	XP_011524106.1:p.Ser344=
XM_017025548.1:c.2599-2784G>A	XP_016881037.1:n.2599-2784G>A
XM_024451084.1:c.1353G>A	XP_024306852.1:p.Ser451=
NM_001384474.1:c.2871G>A MANE Select	NP_001371403.1:p.Ser957=
NM_144612.7:c.2871G>A	NP_653213.6:p.Ser957=