Canonical Allele Identifier: CA343597592

Gene: LHX4 ACBD6 LHX4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180271392C>T , CM000663.2:g.180271392C>T	GRCh38
NC_000001.10:g.180240527C>T , CM000663.1:g.180240527C>T	GRCh37
NC_000001.9:g.178507150C>T	NCBI36
NG_008081.1:g.46086C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_033343.4:c.464C>T (LHX4) MANE Select	NP_203129.1:p.Ala155Val
ENST00000263726.4:c.464C>T (LHX4) MANE Select	ENSP00000263726.2:p.Ala155Val
NM_033343.3:c.464C>T (LHX4)	NP_203129.1:p.Ala155Val
NR_037642.1:n.928G>A (LHX4-AS1)
ENST00000263726.3:c.464C>T (LHX4)	ENSP00000263726.2:p.Ala155Val
ENST00000415414.5:n.928G>A (ACBD6)
ENST00000561113.1:c.401C>T (LHX4)
ENST00000642319.1:c.*1833G>A (ACBD6)	ENSP00000495710.1:n.*1833G>A
ENST00000645415.1:c.*2066G>A (ACBD6)	ENSP00000494507.1:n.*2066G>A
XM_011510105.1:c.281C>T (LHX4)	XP_011508407.1:p.Ala94Val
XM_011510105.2:c.281C>T (LHX4)	XP_011508407.1:p.Ala94Val
XM_011510106.1:c.281C>T (LHX4)	XP_011508408.1:p.Ala94Val
XM_011510106.3:c.281C>T (LHX4)	XP_011508408.1:p.Ala94Val
XM_011510107.1:c.239C>T (LHX4)	XP_011508409.1:p.Ala80Val
XM_011510108.1:c.239C>T (LHX4)	XP_011508410.1:p.Ala80Val
XM_011510108.2:c.239C>T (LHX4)	XP_011508410.1:p.Ala80Val
XM_017002755.1:c.239C>T (LHX4)	XP_016858244.1:p.Ala80Val
XR_001737484.2:n.5355G>A (ACBD6)
XR_001737485.2:n.5338G>A (ACBD6)
XR_002957801.1:n.5257G>A (ACBD6)
XR_921977.3:n.5482G>A (ACBD6)
XR_921978.3:n.5486G>A (ACBD6)