Canonical Allele Identifier: CA402373407

Gene: LOXHD1

Linked Data

• dbSNP Id: rs2035752483
• gnomAD v4: 18-46524838-C-T
• MyVariant Identifiers: chr18:g.44104801C>T (hg19) ; chr18:g.46524838C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46524838C>T , CM000680.2:g.46524838C>T	GRCh38
NC_000018.9:g.44104801C>T , CM000680.1:g.44104801C>T	GRCh37
NC_000018.8:g.42358799C>T	NCBI36
NG_016646.1:g.137196G>A
NG_016646.2:g.137196G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300591.11:c.1277G>A	ENSP00000300591.6:p.Cys426Tyr
ENST00000579038.6:c.989G>A	ENSP00000463285.1:p.Cys330Tyr
ENST00000582408.6:c.1277G>A	ENSP00000461964.1:p.Cys426Tyr
ENST00000642948.1:c.4610G>A MANE Select	ENSP00000496347.1:p.Cys1537Tyr
ENST00000300591.10:c.1277G>A	ENSP00000300591.6:p.Cys426Tyr
ENST00000335730.6:n.3923G>A
ENST00000441551.6:c.3992G>A	ENSP00000387621.2:p.Cys1331Tyr
ENST00000536736.5:c.4610G>A	ENSP00000444586.1:p.Cys1537Tyr
ENST00000579038.5:c.989G>A	ENSP00000463285.1:p.Cys330Tyr
ENST00000582408.5:c.1277G>A	ENSP00000461964.1:p.Cys426Tyr
NM_001145472.2:c.1277G>A	NP_001138944.1:p.Cys426Tyr
NM_001308013.1:c.989G>A	NP_001294942.1:p.Cys330Tyr
NM_144612.6:c.4610G>A	NP_653213.6:p.Cys1537Tyr
XM_006722388.2:c.1409G>A	XP_006722451.1:p.Cys470Tyr
XM_006722389.2:c.1277G>A	XP_006722452.1:p.Cys426Tyr
XM_006722390.2:c.1277G>A	XP_006722453.1:p.Cys426Tyr
XM_006722391.2:c.1409G>A	XP_006722454.1:p.Cys470Tyr
XM_011525803.1:c.4610G>A	XP_011524105.1:p.Cys1537Tyr
XM_011525804.1:c.2771G>A	XP_011524106.1:p.Cys924Tyr
XM_011525805.1:c.1274G>A	XP_011524107.1:p.Cys425Tyr
XM_011525806.1:c.989G>A	XP_011524108.1:p.Cys330Tyr
XM_011525807.1:c.989G>A	XP_011524109.1:p.Cys330Tyr
XM_011525809.1:c.989G>A	XP_011524111.1:p.Cys330Tyr
XM_006722388.3:c.1409G>A	XP_006722451.1:p.Cys470Tyr
XM_006722389.3:c.1277G>A	XP_006722452.1:p.Cys426Tyr
XM_006722390.3:c.1277G>A	XP_006722453.1:p.Cys426Tyr
XM_006722391.3:c.1409G>A	XP_006722454.1:p.Cys470Tyr
XM_011525804.2:c.2771G>A	XP_011524106.1:p.Cys924Tyr
XM_017025548.1:c.3992G>A	XP_016881037.1:p.Cys1331Tyr
XM_024451084.1:c.3092G>A	XP_024306852.1:p.Cys1031Tyr
XM_024451085.1:c.1274G>A	XP_024306853.1:p.Cys425Tyr
XM_024451086.1:c.989G>A	XP_024306854.1:p.Cys330Tyr
XM_024451087.1:c.989G>A	XP_024306855.1:p.Cys330Tyr
XM_024451088.1:c.989G>A	XP_024306856.1:p.Cys330Tyr
NM_001145472.3:c.1277G>A	NP_001138944.1:p.Cys426Tyr
NM_001308013.2:c.989G>A	NP_001294942.1:p.Cys330Tyr
NM_001384474.1:c.4610G>A MANE Select	NP_001371403.1:p.Cys1537Tyr
NM_144612.7:c.4610G>A	NP_653213.6:p.Cys1537Tyr