Canonical Allele Identifier: CA2300898066
Gene: LOXHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46579598G= , CM000680.2:g.46579598G= GRCh38
NC_000018.9:g.44159561G= , CM000680.1:g.44159561G= GRCh37
NC_000018.8:g.42413559G= NCBI36
NG_016646.1:g.82436C=
NG_016646.2:g.82436C=

Transcript Alleles

HGVS Amino-acid change
ENST00000642948.1:c.1809+32C= MANE Select ENSP00000496347.1:n.1809+32C=
ENST00000335730.6:n.1122+32C=
ENST00000441551.6:c.1809+32C= ENSP00000387621.2:n.1809+32C=
ENST00000536736.5:c.1809+32C= ENSP00000444586.1:n.1809+32C=
NM_144612.6:c.1809+32C= NP_653213.6:n.1809+32C=
XM_011525803.1:c.1809+32C= XP_011524105.1:n.1809+32C=
XM_011525804.1:c.-30-1731C= XP_011524106.1:n.-30-1731C=
XM_011525804.2:c.-30-1731C= XP_011524106.1:n.-30-1731C=
XM_017025548.1:c.1809+32C= XP_016881037.1:n.1809+32C=
XM_024451084.1:c.291+32C= XP_024306852.1:n.291+32C=
NM_001384474.1:c.1809+32C= MANE Select NP_001371403.1:n.1809+32C=
NM_144612.7:c.1809+32C= NP_653213.6:n.1809+32C=