Canonical Allele Identifier: CA402373176

Gene: LOXHD1

Linked Data

• gnomAD v4: 18-46524739-T-A
• MyVariant Identifiers: chr18:g.44104702T>A (hg19) ; chr18:g.46524739T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46524739T>A , CM000680.2:g.46524739T>A	GRCh38
NC_000018.9:g.44104702T>A , CM000680.1:g.44104702T>A	GRCh37
NC_000018.8:g.42358700T>A	NCBI36
NG_016646.1:g.137295A>T
NG_016646.2:g.137295A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300591.11:c.1376A>T	ENSP00000300591.6:p.Asp459Val
ENST00000579038.6:c.1088A>T	ENSP00000463285.1:p.Asp363Val
ENST00000582408.6:c.1376A>T	ENSP00000461964.1:p.Asp459Val
ENST00000642948.1:c.4709A>T MANE Select	ENSP00000496347.1:p.Asp1570Val
ENST00000300591.10:c.1376A>T	ENSP00000300591.6:p.Asp459Val
ENST00000335730.6:n.4022A>T
ENST00000441551.6:c.4091A>T	ENSP00000387621.2:p.Asp1364Val
ENST00000536736.5:c.4709A>T	ENSP00000444586.1:p.Asp1570Val
ENST00000579038.5:c.1088A>T	ENSP00000463285.1:p.Asp363Val
ENST00000582408.5:c.1376A>T	ENSP00000461964.1:p.Asp459Val
NM_001145472.2:c.1376A>T	NP_001138944.1:p.Asp459Val
NM_001308013.1:c.1088A>T	NP_001294942.1:p.Asp363Val
NM_144612.6:c.4709A>T	NP_653213.6:p.Asp1570Val
XM_006722388.2:c.1508A>T	XP_006722451.1:p.Asp503Val
XM_006722389.2:c.1376A>T	XP_006722452.1:p.Asp459Val
XM_006722390.2:c.1376A>T	XP_006722453.1:p.Asp459Val
XM_006722391.2:c.1508A>T	XP_006722454.1:p.Asp503Val
XM_011525803.1:c.4709A>T	XP_011524105.1:p.Asp1570Val
XM_011525804.1:c.2870A>T	XP_011524106.1:p.Asp957Val
XM_011525805.1:c.1373A>T	XP_011524107.1:p.Asp458Val
XM_011525806.1:c.1088A>T	XP_011524108.1:p.Asp363Val
XM_011525807.1:c.1088A>T	XP_011524109.1:p.Asp363Val
XM_011525809.1:c.1088A>T	XP_011524111.1:p.Asp363Val
XM_006722388.3:c.1508A>T	XP_006722451.1:p.Asp503Val
XM_006722389.3:c.1376A>T	XP_006722452.1:p.Asp459Val
XM_006722390.3:c.1376A>T	XP_006722453.1:p.Asp459Val
XM_006722391.3:c.1508A>T	XP_006722454.1:p.Asp503Val
XM_011525804.2:c.2870A>T	XP_011524106.1:p.Asp957Val
XM_017025548.1:c.4091A>T	XP_016881037.1:p.Asp1364Val
XM_024451084.1:c.3191A>T	XP_024306852.1:p.Asp1064Val
XM_024451085.1:c.1373A>T	XP_024306853.1:p.Asp458Val
XM_024451086.1:c.1088A>T	XP_024306854.1:p.Asp363Val
XM_024451087.1:c.1088A>T	XP_024306855.1:p.Asp363Val
XM_024451088.1:c.1088A>T	XP_024306856.1:p.Asp363Val
NM_001145472.3:c.1376A>T	NP_001138944.1:p.Asp459Val
NM_001308013.2:c.1088A>T	NP_001294942.1:p.Asp363Val
NM_001384474.1:c.4709A>T MANE Select	NP_001371403.1:p.Asp1570Val
NM_144612.7:c.4709A>T	NP_653213.6:p.Asp1570Val