Canonical Allele Identifier: CA402373226

Gene: LOXHD1

Linked Data

• MyVariant Identifiers: chr18:g.44104723C>G (hg19) ; chr18:g.46524760C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46524760C>G , CM000680.2:g.46524760C>G	GRCh38
NC_000018.9:g.44104723C>G , CM000680.1:g.44104723C>G	GRCh37
NC_000018.8:g.42358721C>G	NCBI36
NG_016646.1:g.137274G>C
NG_016646.2:g.137274G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300591.11:c.1355G>C	ENSP00000300591.6:p.Trp452Ser
ENST00000579038.6:c.1067G>C	ENSP00000463285.1:p.Trp356Ser
ENST00000582408.6:c.1355G>C	ENSP00000461964.1:p.Trp452Ser
ENST00000642948.1:c.4688G>C MANE Select	ENSP00000496347.1:p.Trp1563Ser
ENST00000300591.10:c.1355G>C	ENSP00000300591.6:p.Trp452Ser
ENST00000335730.6:n.4001G>C
ENST00000441551.6:c.4070G>C	ENSP00000387621.2:p.Trp1357Ser
ENST00000536736.5:c.4688G>C	ENSP00000444586.1:p.Trp1563Ser
ENST00000579038.5:c.1067G>C	ENSP00000463285.1:p.Trp356Ser
ENST00000582408.5:c.1355G>C	ENSP00000461964.1:p.Trp452Ser
NM_001145472.2:c.1355G>C	NP_001138944.1:p.Trp452Ser
NM_001308013.1:c.1067G>C	NP_001294942.1:p.Trp356Ser
NM_144612.6:c.4688G>C	NP_653213.6:p.Trp1563Ser
XM_006722388.2:c.1487G>C	XP_006722451.1:p.Trp496Ser
XM_006722389.2:c.1355G>C	XP_006722452.1:p.Trp452Ser
XM_006722390.2:c.1355G>C	XP_006722453.1:p.Trp452Ser
XM_006722391.2:c.1487G>C	XP_006722454.1:p.Trp496Ser
XM_011525803.1:c.4688G>C	XP_011524105.1:p.Trp1563Ser
XM_011525804.1:c.2849G>C	XP_011524106.1:p.Trp950Ser
XM_011525805.1:c.1352G>C	XP_011524107.1:p.Trp451Ser
XM_011525806.1:c.1067G>C	XP_011524108.1:p.Trp356Ser
XM_011525807.1:c.1067G>C	XP_011524109.1:p.Trp356Ser
XM_011525809.1:c.1067G>C	XP_011524111.1:p.Trp356Ser
XM_006722388.3:c.1487G>C	XP_006722451.1:p.Trp496Ser
XM_006722389.3:c.1355G>C	XP_006722452.1:p.Trp452Ser
XM_006722390.3:c.1355G>C	XP_006722453.1:p.Trp452Ser
XM_006722391.3:c.1487G>C	XP_006722454.1:p.Trp496Ser
XM_011525804.2:c.2849G>C	XP_011524106.1:p.Trp950Ser
XM_017025548.1:c.4070G>C	XP_016881037.1:p.Trp1357Ser
XM_024451084.1:c.3170G>C	XP_024306852.1:p.Trp1057Ser
XM_024451085.1:c.1352G>C	XP_024306853.1:p.Trp451Ser
XM_024451086.1:c.1067G>C	XP_024306854.1:p.Trp356Ser
XM_024451087.1:c.1067G>C	XP_024306855.1:p.Trp356Ser
XM_024451088.1:c.1067G>C	XP_024306856.1:p.Trp356Ser
NM_001145472.3:c.1355G>C	NP_001138944.1:p.Trp452Ser
NM_001308013.2:c.1067G>C	NP_001294942.1:p.Trp356Ser
NM_001384474.1:c.4688G>C MANE Select	NP_001371403.1:p.Trp1563Ser
NM_144612.7:c.4688G>C	NP_653213.6:p.Trp1563Ser