Canonical Allele Identifier: CA402379121

Gene: LOXHD1

Linked Data

• MyVariant Identifiers: chr18:g.44159717C>T (hg19) ; chr18:g.46579754C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46579754C>T , CM000680.2:g.46579754C>T	GRCh38
NC_000018.9:g.44159717C>T , CM000680.1:g.44159717C>T	GRCh37
NC_000018.8:g.42413715C>T	NCBI36
NG_016646.1:g.82280G>A
NG_016646.2:g.82280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642948.1:c.1685G>A MANE Select	ENSP00000496347.1:p.Gly562Asp
ENST00000335730.6:n.998G>A
ENST00000441551.6:c.1685G>A	ENSP00000387621.2:p.Gly562Asp
ENST00000536736.5:c.1685G>A	ENSP00000444586.1:p.Gly562Asp
NM_144612.6:c.1685G>A	NP_653213.6:p.Gly562Asp
XM_011525803.1:c.1685G>A	XP_011524105.1:p.Gly562Asp
XM_011525804.1:c.-30-1887G>A	XP_011524106.1:n.-30-1887G>A
XM_011525804.2:c.-30-1887G>A	XP_011524106.1:n.-30-1887G>A
XM_017025548.1:c.1685G>A	XP_016881037.1:p.Gly562Asp
XM_024451084.1:c.167G>A	XP_024306852.1:p.Gly56Asp
NM_001384474.1:c.1685G>A MANE Select	NP_001371403.1:p.Gly562Asp
NM_144612.7:c.1685G>A	NP_653213.6:p.Gly562Asp