Canonical Allele Identifier: CA1272033

Gene: LHX4 ACBD6 LHX4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180274252C>T , CM000663.2:g.180274252C>T	GRCh38
NC_000001.10:g.180243387C>T , CM000663.1:g.180243387C>T	GRCh37
NC_000001.9:g.178510010C>T	NCBI36
NG_008081.1:g.48946C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.846C>T (LHX4) MANE Select	ENSP00000263726.2:p.Gly282=
ENST00000642319.1:c.*937-140G>A (ACBD6)	ENSP00000495710.1:n.*937-140G>A
ENST00000645415.1:c.*1170-140G>A (ACBD6)	ENSP00000494507.1:n.*1170-140G>A
ENST00000263726.3:c.846C>T (LHX4)	ENSP00000263726.2:p.Gly282=
ENST00000415414.5:n.32-140G>A (ACBD6)
ENST00000440959.2:n.1575-140G>A (ACBD6)
ENST00000622400.1:n.64-140G>A (ACBD6)
NM_033343.3:c.846C>T (LHX4)	NP_203129.1:p.Gly282=
NR_037642.1:n.32-140G>A (LHX4-AS1)
XM_011510105.1:c.663C>T (LHX4)	XP_011508407.1:p.Gly221=
XM_011510106.1:c.663C>T (LHX4)	XP_011508408.1:p.Gly221=
XM_011510107.1:c.621C>T (LHX4)	XP_011508409.1:p.Gly207=
XM_011510108.1:c.621C>T (LHX4)	XP_011508410.1:p.Gly207=
XM_011510105.2:c.663C>T (LHX4)	XP_011508407.1:p.Gly221=
XM_011510106.3:c.663C>T (LHX4)	XP_011508408.1:p.Gly221=
XM_011510108.2:c.621C>T (LHX4)	XP_011508410.1:p.Gly207=
XM_017002755.1:c.621C>T (LHX4)	XP_016858244.1:p.Gly207=
XR_001737484.2:n.2495G>A (ACBD6)
XR_001737485.2:n.2478G>A (ACBD6)
XR_002957801.1:n.2397G>A (ACBD6)
XR_921977.3:n.2622G>A (ACBD6)
XR_921978.3:n.2626G>A (ACBD6)
NM_033343.4:c.846C>T (LHX4) MANE Select	NP_203129.1:p.Gly282=