Canonical Allele Identifier: CA1272081

Gene: LHX4 ACBD6 LHX4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180274476G>A , CM000663.2:g.180274476G>A	GRCh38
NC_000001.10:g.180243611G>A , CM000663.1:g.180243611G>A	GRCh37
NC_000001.9:g.178510234G>A	NCBI36
NG_008081.1:g.49170G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_033343.4:c.1070G>A (LHX4) MANE Select	NP_203129.1:p.Gly357Glu
ENST00000263726.4:c.1070G>A (LHX4) MANE Select	ENSP00000263726.2:p.Gly357Glu
NM_033343.3:c.1070G>A (LHX4)	NP_203129.1:p.Gly357Glu
NR_037642.1:n.31+175C>T (LHX4-AS1)
ENST00000263726.3:c.1070G>A (LHX4)	ENSP00000263726.2:p.Gly357Glu
ENST00000415414.5:n.31+175C>T (ACBD6)
ENST00000440959.2:n.1574+175C>T (ACBD6)
ENST00000622400.1:n.63+175C>T (ACBD6)
ENST00000642319.1:c.*936+175C>T (ACBD6)	ENSP00000495710.1:n.*936+175C>T
ENST00000645415.1:c.*1169+175C>T (ACBD6)	ENSP00000494507.1:n.*1169+175C>T
XM_011510105.1:c.887G>A (LHX4)	XP_011508407.1:p.Gly296Glu
XM_011510105.2:c.887G>A (LHX4)	XP_011508407.1:p.Gly296Glu
XM_011510106.1:c.887G>A (LHX4)	XP_011508408.1:p.Gly296Glu
XM_011510106.3:c.887G>A (LHX4)	XP_011508408.1:p.Gly296Glu
XM_011510107.1:c.845G>A (LHX4)	XP_011508409.1:p.Gly282Glu
XM_011510108.1:c.845G>A (LHX4)	XP_011508410.1:p.Gly282Glu
XM_011510108.2:c.845G>A (LHX4)	XP_011508410.1:p.Gly282Glu
XM_017002755.1:c.845G>A (LHX4)	XP_016858244.1:p.Gly282Glu
XR_001737484.2:n.2271C>T (ACBD6)
XR_001737485.2:n.2254C>T (ACBD6)
XR_002957801.1:n.2173C>T (ACBD6)
XR_921977.3:n.2398C>T (ACBD6)
XR_921978.3:n.2402C>T (ACBD6)