Canonical Allele Identifier: CA1272059

Gene: LHX4 ACBD6 LHX4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180274375C>T , CM000663.2:g.180274375C>T	GRCh38
NC_000001.10:g.180243510C>T , CM000663.1:g.180243510C>T	GRCh37
NC_000001.9:g.178510133C>T	NCBI36
NG_008081.1:g.49069C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.969C>T (LHX4) MANE Select	ENSP00000263726.2:p.His323=
ENST00000642319.1:c.*937-263G>A (ACBD6)	ENSP00000495710.1:n.*937-263G>A
ENST00000645415.1:c.*1170-263G>A (ACBD6)	ENSP00000494507.1:n.*1170-263G>A
ENST00000263726.3:c.969C>T (LHX4)	ENSP00000263726.2:p.His323=
ENST00000415414.5:n.32-263G>A (ACBD6)
ENST00000440959.2:n.1575-263G>A (ACBD6)
ENST00000622400.1:n.64-263G>A (ACBD6)
NM_033343.3:c.969C>T (LHX4)	NP_203129.1:p.His323=
NR_037642.1:n.32-263G>A (LHX4-AS1)
XM_011510105.1:c.786C>T (LHX4)	XP_011508407.1:p.His262=
XM_011510106.1:c.786C>T (LHX4)	XP_011508408.1:p.His262=
XM_011510107.1:c.744C>T (LHX4)	XP_011508409.1:p.His248=
XM_011510108.1:c.744C>T (LHX4)	XP_011508410.1:p.His248=
XM_011510105.2:c.786C>T (LHX4)	XP_011508407.1:p.His262=
XM_011510106.3:c.786C>T (LHX4)	XP_011508408.1:p.His262=
XM_011510108.2:c.744C>T (LHX4)	XP_011508410.1:p.His248=
XM_017002755.1:c.744C>T (LHX4)	XP_016858244.1:p.His248=
XR_001737484.2:n.2372G>A (ACBD6)
XR_001737485.2:n.2355G>A (ACBD6)
XR_002957801.1:n.2274G>A (ACBD6)
XR_921977.3:n.2499G>A (ACBD6)
XR_921978.3:n.2503G>A (ACBD6)
NM_033343.4:c.969C>T (LHX4) MANE Select	NP_203129.1:p.His323=