Canonical Allele Identifier: CA402376225

Gene: LOXHD1

Linked Data

• MyVariant Identifiers: chr18:g.44152047A>C (hg19) ; chr18:g.46572084A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46572084A>C , CM000680.2:g.46572084A>C	GRCh38
NC_000018.9:g.44152047A>C , CM000680.1:g.44152047A>C	GRCh37
NC_000018.8:g.42406045A>C	NCBI36
NG_016646.1:g.89950T>G
NG_016646.2:g.89950T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642948.1:c.2047+2T>G MANE Select	ENSP00000496347.1:n.2047+2T>G
ENST00000335730.6:n.1360+2T>G
ENST00000441551.6:c.2047+2T>G	ENSP00000387621.2:n.2047+2T>G
ENST00000536736.5:c.2047+2T>G	ENSP00000444586.1:n.2047+2T>G
NM_144612.6:c.2047+2T>G	NP_653213.6:n.2047+2T>G
XM_011525803.1:c.2047+2T>G	XP_011524105.1:n.2047+2T>G
XM_011525804.1:c.208+2T>G	XP_011524106.1:n.208+2T>G
XM_011525804.2:c.208+2T>G	XP_011524106.1:n.208+2T>G
XM_017025548.1:c.2047+2T>G	XP_016881037.1:n.2047+2T>G
XM_024451084.1:c.529+2T>G	XP_024306852.1:n.529+2T>G
NM_001384474.1:c.2047+2T>G MANE Select	NP_001371403.1:n.2047+2T>G
NM_144612.7:c.2047+2T>G	NP_653213.6:n.2047+2T>G