Canonical Allele Identifier: CA1272034

Gene: LHX4 ACBD6 LHX4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180274253G>A , CM000663.2:g.180274253G>A	GRCh38
NC_000001.10:g.180243388G>A , CM000663.1:g.180243388G>A	GRCh37
NC_000001.9:g.178510011G>A	NCBI36
NG_008081.1:g.48947G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.847G>A (LHX4) MANE Select	ENSP00000263726.2:p.Gly283Arg
ENST00000642319.1:c.*937-141C>T (ACBD6)	ENSP00000495710.1:n.*937-141C>T
ENST00000645415.1:c.*1170-141C>T (ACBD6)	ENSP00000494507.1:n.*1170-141C>T
ENST00000263726.3:c.847G>A (LHX4)	ENSP00000263726.2:p.Gly283Arg
ENST00000415414.5:n.32-141C>T (ACBD6)
ENST00000440959.2:n.1575-141C>T (ACBD6)
ENST00000622400.1:n.64-141C>T (ACBD6)
NM_033343.3:c.847G>A (LHX4)	NP_203129.1:p.Gly283Arg
NR_037642.1:n.32-141C>T (LHX4-AS1)
XM_011510105.1:c.664G>A (LHX4)	XP_011508407.1:p.Gly222Arg
XM_011510106.1:c.664G>A (LHX4)	XP_011508408.1:p.Gly222Arg
XM_011510107.1:c.622G>A (LHX4)	XP_011508409.1:p.Gly208Arg
XM_011510108.1:c.622G>A (LHX4)	XP_011508410.1:p.Gly208Arg
XM_011510105.2:c.664G>A (LHX4)	XP_011508407.1:p.Gly222Arg
XM_011510106.3:c.664G>A (LHX4)	XP_011508408.1:p.Gly222Arg
XM_011510108.2:c.622G>A (LHX4)	XP_011508410.1:p.Gly208Arg
XM_017002755.1:c.622G>A (LHX4)	XP_016858244.1:p.Gly208Arg
XR_001737484.2:n.2494C>T (ACBD6)
XR_001737485.2:n.2477C>T (ACBD6)
XR_002957801.1:n.2396C>T (ACBD6)
XR_921977.3:n.2621C>T (ACBD6)
XR_921978.3:n.2625C>T (ACBD6)
NM_033343.4:c.847G>A (LHX4) MANE Select	NP_203129.1:p.Gly283Arg