Canonical Allele Identifier: CA402376269
Gene: LOXHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46572095T>A , CM000680.2:g.46572095T>A GRCh38
NC_000018.9:g.44152058T>A , CM000680.1:g.44152058T>A GRCh37
NC_000018.8:g.42406056T>A NCBI36
NG_016646.1:g.89939A>T
NG_016646.2:g.89939A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642948.1:c.2038A>T MANE Select ENSP00000496347.1:p.Thr680Ser
ENST00000335730.6:n.1351A>T
ENST00000441551.6:c.2038A>T ENSP00000387621.2:p.Thr680Ser
ENST00000536736.5:c.2038A>T ENSP00000444586.1:p.Thr680Ser
NM_144612.6:c.2038A>T NP_653213.6:p.Thr680Ser
XM_011525803.1:c.2038A>T XP_011524105.1:p.Thr680Ser
XM_011525804.1:c.199A>T XP_011524106.1:p.Thr67Ser
XM_011525804.2:c.199A>T XP_011524106.1:p.Thr67Ser
XM_017025548.1:c.2038A>T XP_016881037.1:p.Thr680Ser
XM_024451084.1:c.520A>T XP_024306852.1:p.Thr174Ser
NM_001384474.1:c.2038A>T MANE Select NP_001371403.1:p.Thr680Ser
NM_144612.7:c.2038A>T NP_653213.6:p.Thr680Ser