Canonical Allele Identifier: CA1143628257

Gene: LHX4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266508G= , CM000663.2:g.180266508G=	GRCh38
NC_000001.10:g.180235643G= , CM000663.1:g.180235643G=	GRCh37
NC_000001.9:g.178502266G=	NCBI36
NG_008081.1:g.41202G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.365G= MANE Select	ENSP00000263726.2:p.Arg122=
ENST00000263726.3:c.365G=	ENSP00000263726.2:p.Arg122=
ENST00000561113.1:c.302G=
NM_033343.3:c.365G=	NP_203129.1:p.Arg122=
XM_011510105.1:c.182G=	XP_011508407.1:p.Arg61=
XM_011510106.1:c.182G=	XP_011508408.1:p.Arg61=
XM_011510107.1:c.140G=	XP_011508409.1:p.Arg47=
XM_011510108.1:c.140G=	XP_011508410.1:p.Arg47=
XM_011510105.2:c.182G=	XP_011508407.1:p.Arg61=
XM_011510106.3:c.182G=	XP_011508408.1:p.Arg61=
XM_011510108.2:c.140G=	XP_011508410.1:p.Arg47=
XM_017002755.1:c.140G=	XP_016858244.1:p.Arg47=
NM_033343.4:c.365G= MANE Select	NP_203129.1:p.Arg122=