Canonical Allele Identifier: CA1272099

Gene: LHX4 ACBD6 LHX4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180274566A>C , CM000663.2:g.180274566A>C	GRCh38
NC_000001.10:g.180243701A>C , CM000663.1:g.180243701A>C	GRCh37
NC_000001.9:g.178510324A>C	NCBI36
NG_008081.1:g.49260A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_033343.4:c.1160A>C (LHX4) MANE Select	NP_203129.1:p.His387Pro
ENST00000263726.4:c.1160A>C (LHX4) MANE Select	ENSP00000263726.2:p.His387Pro
NM_033343.3:c.1160A>C (LHX4)	NP_203129.1:p.His387Pro
NR_037642.1:n.31+85T>G (LHX4-AS1)
ENST00000263726.3:c.1160A>C (LHX4)	ENSP00000263726.2:p.His387Pro
ENST00000415414.5:n.31+85T>G (ACBD6)
ENST00000440959.2:n.1574+85T>G (ACBD6)
ENST00000622400.1:n.63+85T>G (ACBD6)
ENST00000642319.1:c.*936+85T>G (ACBD6)	ENSP00000495710.1:n.*936+85T>G
ENST00000645415.1:c.*1169+85T>G (ACBD6)	ENSP00000494507.1:n.*1169+85T>G
XM_011510105.1:c.977A>C (LHX4)	XP_011508407.1:p.His326Pro
XM_011510105.2:c.977A>C (LHX4)	XP_011508407.1:p.His326Pro
XM_011510106.1:c.977A>C (LHX4)	XP_011508408.1:p.His326Pro
XM_011510106.3:c.977A>C (LHX4)	XP_011508408.1:p.His326Pro
XM_011510107.1:c.935A>C (LHX4)	XP_011508409.1:p.His312Pro
XM_011510108.1:c.935A>C (LHX4)	XP_011508410.1:p.His312Pro
XM_011510108.2:c.935A>C (LHX4)	XP_011508410.1:p.His312Pro
XM_017002755.1:c.935A>C (LHX4)	XP_016858244.1:p.His312Pro
XR_001737484.2:n.2181T>G (ACBD6)
XR_001737485.2:n.2164T>G (ACBD6)
XR_002957801.1:n.2083T>G (ACBD6)
XR_921977.3:n.2308T>G (ACBD6)
XR_921978.3:n.2312T>G (ACBD6)